111306001: Multiple lentigines syndrome (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lentiginosis\Multiple lentigines syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome

\Mass of body structure\Lentiginosis\Multiple lentigines syndrome

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Multiple lentigines syndrome
\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Multiple lentigines syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Multiple lentigines syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Multiple lentigines syndrome
\Disease\Disorder of pigmentation (disorder)\Melanosis (disorder)\Lentiginosis\Multiple lentigines syndrome
\Disease\Disorder of foetus and/or newborn\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\Disease\Neoplasm and/or hamartoma (disorder)\Hamartoma (disorder)\Lentiginosis\Multiple lentigines syndrome
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Multiple lentigines syndrome
\Disease\Disorder of body system\Skin or mucosa lesion\Lentiginosis\Multiple lentigines syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Multiple lentigines syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Multiple lentigines syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple lentigines syndrome

Status: current, Not 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
Multiple lentigines syndrome	Is a	Hamartomatous disease	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Lentigo	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Congenital anomaly of skin (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Associated morphology	naevus pigmentaire	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Pathological process	Benign neoplastic process	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Associated morphology	Hyperpigmentation (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Is a	Benign neoplasm of skin (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Is a	lentigo	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Acquired melanocytic nevus	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Melanocytic naevus of skin	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Melanocytic tumor of skin	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Associated morphology	Hamartoma	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Is a	Neoplasm of skin region	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Associated morphology	Structure showing abnormal deposition of pigment (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Hereditary disorder of the integument (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Associated morphology	Increased melanin pigmentation	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Is a	Genetic disorder of skin pigmentation (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Lentiginosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Associated morphology	Lentigo	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Is a	Mass of soft tissue	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Finding site	Skin and/or subcutaneous tissue structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Is a	Lesion of soft tissue (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Finding site	Structure of skin and/or mucous membrane (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Is a	Hamartoma of integument (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Is a	Mass of body region (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple lentigines syndrome	Associated morphology	Lentigo	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Finding site	Skin and/or subcutaneous tissue structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Associated morphology	Lentigo	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Multiple lentigines syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple lentigines syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple lentigines syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
178538018	Multiple lentigines syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
187732010	LEOPARD syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
630152013	Multiple lentigines syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1219626017	Leopard syndrome lentiginosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
178538018	Multiple lentigines syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
178538018	Multiple lentigines syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
187732010	LEOPARD syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
630152013	Multiple lentigines syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
630152013	Multiple lentigines syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1215882014	Generalised lentiginosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1217385016	Generalized lentiginosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1219626017	Leopard syndrome lentiginosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1219626017	Leopard syndrome lentiginosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1219627014	Leopard syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1219627014	Leopard syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3454371001000119	Noonan-Syndrom mit multiplen Lentigines	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6050591000241111	lentiginose cardiomyopathique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6050601000241116	syndrome léopard	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6050611000241119	syndrome de Noonan avec lentigines multiples	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6050591000241111	lentiginose cardiomyopathique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6050601000241116	syndrome léopard	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6050611000241119	syndrome de Noonan avec lentigines multiples	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3454371001000119	Noonan-Syndrom mit multiplen Lentigines	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module