54411001: Peutz-Jeghers syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lentiginosis\Peutz-Jeghers syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Mass of skin\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome

\Viscus structure finding (finding)\Abdominal organ finding\Bowel finding\Disease of intestine\...

\Hamartoma of intestine\Peutz-Jeghers syndrome

\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome

\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Bowel finding\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Gastrointestinal tract finding (finding)\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Mass of digestive structure\Hamartoma of intestine\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Mass of digestive structure\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Digestive system hereditary disorder\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Digestive system finding (finding)\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Peutz-Jeghers syndrome

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Hamartoma of intestine\Peutz-Jeghers syndrome
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Bowel finding\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disease of abdomen\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Hamartoma of intestine\Peutz-Jeghers syndrome
\Finding of trunk structure\Mass of trunk (finding)\Abdominal mass\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome

\Mass of body structure\Mass of soft tissue\Neoplasm of soft tissue (disorder)\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Mass of body structure\Mass of soft tissue\Mass of skin\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Mass of body structure\Lentiginosis\Peutz-Jeghers syndrome
\Mass of body structure\Neoplasm of integumentary system\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Hamartoma of intestine\Peutz-Jeghers syndrome
\Mass of body structure\Mass of body region (finding)\Mass of trunk (finding)\Abdominal mass\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Mass of body structure\Mass of body region (finding)\Mass of skin\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Mass of body structure\Mass of digestive structure\Hamartoma of intestine\Peutz-Jeghers syndrome
\Mass of body structure\Mass of digestive structure\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Mass of body structure\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neurocutaneous syndrome\Peutz-Jeghers syndrome

\Neurological lesion\Space-occupying lesion of nervous system\Neoplasm of nervous system\Neurocutaneous syndrome\Peutz-Jeghers syndrome

\General finding of soft tissue\Mass of soft tissue\Neoplasm of soft tissue (disorder)\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\General finding of soft tissue\Mass of soft tissue\Mass of skin\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\General finding of soft tissue\Skin finding\Mass of skin\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Neoplasm of soft tissue (disorder)\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome

\Integumentary system finding\Disorder of integument\Neoplasm of integumentary system\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Peutz-Jeghers syndrome
\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Integumentary system finding\Skin finding\Mass of skin\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary cancer-predisposing syndrome\Peutz-Jeghers syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Peutz-Jeghers syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Peutz-Jeghers syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Peutz-Jeghers syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Peutz-Jeghers syndrome
\Disease\Polyp (disorder)\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of pigmentation (disorder)\Melanosis (disorder)\Lentiginosis\Peutz-Jeghers syndrome
\Disease\Disorder of pigmentation (disorder)\Melanosis (disorder)\Congenital melanosis (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of foetus and/or newborn\Disorder involving the integument of fetus OR newborn\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital hamartoma (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital melanosis (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of foetus and/or newborn\Disorder of digestive system specific to fetus OR newborn\Peutz-Jeghers syndrome
\Disease\Neoplasm and/or hamartoma (disorder)\Hamartoma (disorder)\Lentiginosis\Peutz-Jeghers syndrome
\Disease\Neoplasm and/or hamartoma (disorder)\Hamartoma (disorder)\Congenital hamartoma (disorder)\Peutz-Jeghers syndrome
\Disease\Neoplasm and/or hamartoma (disorder)\Hamartoma (disorder)\Hamartoma of intestine\Peutz-Jeghers syndrome
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of integumentary system\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of soft tissue (disorder)\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of nervous system\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of nervous system (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Digestive system hereditary disorder\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Skin or mucosa lesion\Lentiginosis\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disorder of integument\Neoplasm of integumentary system\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder involving the integument of fetus OR newborn\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Hereditary disorder of nervous system (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of nervous system (disorder)\Neoplasm of nervous system\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Digestive system hereditary disorder\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive tract\Disorder of gastrointestinal tract (disorder)\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive organ\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of body system\Disease of digestive system (disorder)\Disorder of digestive system specific to fetus OR newborn\Peutz-Jeghers syndrome
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Hamartoma of intestine\Peutz-Jeghers syndrome
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disease of intestine\Polyp of intestine\Intestinal polyposis syndrome (disorder)\Peutz-Jeghers syndrome
\Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Neoplasm of soft tissue (disorder)\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Neoplasm of skin\Neurocutaneous syndrome\Peutz-Jeghers syndrome

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Peutz-Jeghers syndrome	Is a	Intestinal polyposis syndrome (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Familial disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Congenital anomaly of the haematopoietic system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Benign neoplasm of trunk	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Lentigo	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Iron deficiency anemia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Congenital anomaly of digestive system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Hereditary disorder of haematologic sysem	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Neurocutaneous syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Congenital anomaly of trunk	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Associated morphology	Hyperpigmentation (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Associated morphology	Dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Pathological process	Benign neoplastic process	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Finding site	Nervous system structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Associated morphology	Melanosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Interprets	Nutritional deficiency state	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Finding site	Intestinal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Interprets	Decreased erythrocyte production	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Associated morphology	Hamartomatous polyp	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Associated morphology	naevus pigmentaire	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Is a	Neoplasm of nervous system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Is a	Congenital hamartoma (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	lentigo	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Associated morphology	Neoplasm	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Is a	Hamartoma of intestine	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Disorder of soft tissue of body cavity	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Associated morphology	Structure showing abnormal deposition of pigment (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Is a	Melanosis (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Disorder of skin pigmentation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Associated morphology	Melanin pigmentation	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Is a	Degenerative disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Associated morphology	Peutz Jeghers polyp (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Finding site	Intestinal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Is a	Disorder of soft tissue of body cavity	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Peutz-Jeghers syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Peutz-Jeghers syndrome	Finding site	Nervous system structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Peutz-Jeghers syndrome	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Hereditary disorder of the integument (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Genetic disorder of skin pigmentation (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Congenital hamartoma of skin (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Congenital anomaly of intestinal tract	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Lentiginosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Is a	Congenital pigmentary skin anomalies	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Associated morphology	Lentigo	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Associated morphology	Peutz Jeghers polyp (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Finding site	Intestinal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Is a	Congenital melanosis (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Finding site	Structure of skin and/or mucous membrane (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Peutz-Jeghers syndrome	Is a	Hereditary cancer-predisposing syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Is a	Developmental hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Peutz-Jeghers syndrome	Associated morphology	Neoplasm	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Peutz-Jeghers syndrome	Associated morphology	Neoplasm	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Peutz-Jeghers syndrome	Finding site	Structure of skin and/or mucous membrane (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Associated morphology	Lentigo	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Peutz-Jeghers syndrome	Is a	Disorder of digestive system specific to fetus OR newborn	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Peutz-Jeghers polyps of small bowel	Is a	True	Peutz-Jeghers syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
90442013	Peutz-Jeghers syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
90443015	Periorificial lentiginosis syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
792640014	Peutz-Jeghers syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1231333015	Perioral lentiginosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1231335010	Peutz-Jeghers polyposis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3880767012	PJS - Peutz-Jeghers syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
90442013	Peutz-Jeghers syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
90443015	Periorificial lentiginosis syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
90443015	Periorificial lentiginosis syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
792640014	Peutz-Jeghers syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
792640014	Peutz-Jeghers syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1231333015	Perioral lentiginosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1231333015	Perioral lentiginosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1231334014	PJS - Peutz-Jehgers syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1231334014	PJS - Peutz-Jehgers syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1231335010	Peutz-Jeghers polyposis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1231335010	Peutz-Jeghers polyposis	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3880767012	PJS - Peutz-Jeghers syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3389331001000115	Peutz-Jeghers-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
125901000077112	lentiginose périorificielle avec polypose viscérale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
953801000172113	syndrome de Peutz-Jeghers	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1005121000172111	PJS - Peutz-Jeghers syndrome	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
125901000077112	lentiginose périorificielle avec polypose viscérale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
953801000172113	syndrome de Peutz-Jeghers	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1005121000172111	PJS - Peutz-Jeghers syndrome	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3389331001000115	Peutz-Jeghers-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module