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1953005: Congenital deficiency of pigment of skin (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4374015 Congenital deficiency of pigment of skin en Synonym Active Entire term case insensitive SNOMED CT core module
747753014 Congenital deficiency of pigment of skin (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


34 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital deficiency of pigment of skin Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Is a Skin lesion false Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Congenital deficiency of pigment of skin Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital deficiency of pigment of skin Is a Congenital pigmentary anomaly of skin false Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Is a Hypopigmentation of skin true Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital deficiency of pigment of skin Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Congenital deficiency of pigment of skin Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Congenital deficiency of pigment of skin Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
Congenital deficiency of pigment of skin Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Congenital deficiency of pigment of skin Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital deficiency of pigment of skin Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Congenital deficiency of pigment of skin Is a Congenital pigmentary skin anomalies true Inferred relationship Existential restriction modifier
Congenital deficiency of pigment of skin Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital deficiency of pigment of skin Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Albinism Is a False Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a False Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Albinoidism Is a False Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a False Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Waardenburg syndrome type 3 Is a False Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Oculocerebral hypopigmentation syndrome of Preus type Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Piebaldism Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Deaf blind hypopigmentation syndrome Yemenite type Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Albinism with deafness syndrome Is a False Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Waardenburg syndrome Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Piebald trait with neurologic defects syndrome Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Phylloid hypomelanosis Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Is a True Congenital deficiency of pigment of skin Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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