83145004: Abnormal dermatoglyphic pattern (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)
\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)\Abnormal dermatoglyphic pattern (disorder)

\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)

\Disease\Disorder of foetus and/or newborn\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)
\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)\Abnormal dermatoglyphic pattern (disorder)
\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)\Abnormal dermatoglyphic pattern (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Abnormal dermatoglyphic pattern (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Abnormal dermatoglyphic pattern (disorder)	Is a	Congenital anomaly of skin (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Abnormal dermatoglyphic pattern (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Abnormal dermatoglyphic pattern (disorder)	Finding site	Structure of dermatoglyphic patterns (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Abnormal dermatoglyphic pattern (disorder)	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Abnormal dermatoglyphic pattern (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Abnormal dermatoglyphic pattern (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Abnormal dermatoglyphic pattern (disorder)	Finding site	Structure of dermatoglyphic patterns (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Abnormal dermatoglyphic pattern (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Abnormal dermatoglyphic pattern (disorder)	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Abnormal dermatoglyphic pattern (disorder)	Finding site	Structure of dermatoglyphic patterns (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Abnormal dermatoglyphic pattern (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Abnormal dermatoglyphic pattern (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Abnormal dermatoglyphic pattern (disorder)	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Abnormal palmar creases (disorder)	Is a	True	Abnormal dermatoglyphic pattern (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Abnormal plantar creases	Is a	True	Abnormal dermatoglyphic pattern (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dermatoglyphs - skin lines	Is a	True	Abnormal dermatoglyphic pattern (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dermatoglyphic anomalies NOS	Is a	False	Abnormal dermatoglyphic pattern (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
A rare syndrome characterized by neonatal blisters and milia (small white papules, especially on the face) and congenital absence of dermatoglyphics on the hands and feet. It has been reported in two kindreds (one of which contained 13 affected individuals spanning three generations) and in an unrelated individual. Some affected patients also showed bilateral partial flexion contractures of the fingers and toes, and webbing of the toes. The syndrome is inherited as an autosomal dominant trait.	Is a	True	Abnormal dermatoglyphic pattern (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Isolated congenital adermatoglyphia is a rare, genetic developmental defect during embryogenesis disorder characterised by the lack of epidermal ridges on the palms and soles, resulting in the absence of fingerprints, with no other associated manifestations. It is associated with a reduced number of sweat gland openings and reduced transpiration of palms and soles.	Is a	True	Abnormal dermatoglyphic pattern (disorder)	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
137907016	Abnormal dermatoglyphic pattern	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
505463018	Dermatoglyphic anomalies	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
505464012	Dermatoglyphic abnormality	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
824717012	Abnormal dermatoglyphic pattern (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
137907016	Abnormal dermatoglyphic pattern	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
137907016	Abnormal dermatoglyphic pattern	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
505463018	Dermatoglyphic anomalies	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
505463018	Dermatoglyphic anomalies	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
505464012	Dermatoglyphic abnormality	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
505464012	Dermatoglyphic abnormality	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
824717012	Abnormal dermatoglyphic pattern (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
824717012	Abnormal dermatoglyphic pattern (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4661471000241114	anomalies congénitale des dermatoglyphes	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4661471000241114	anomalies congénitale des dermatoglyphes	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module