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61649007: Congenital oculocutaneous hypopigmentation (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
102437010 Congenital oculocutaneous hypopigmentation en Synonym Active Entire term case insensitive SNOMED CT core module
800734016 Congenital oculocutaneous hypopigmentation (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


22 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of eye true Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Finding site Structure of eye proper true Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Is a Disorder of eye region false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Is a Ear, face and neck congenital anomalies false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Is a Skin lesion false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Finding site Eye region structure false Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Is a Congenital deficiency of pigment of skin true Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Finding site Eye region structure false Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital oculocutaneous hypopigmentation Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital oculocutaneous hypopigmentation Finding site Structure of integumentary system false Inferred relationship Existential restriction modifier 2
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Is a Hypopigmentation of skin false Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Congenital oculocutaneous hypopigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 3
Congenital oculocutaneous hypopigmentation Is a Lesion of eye true Inferred relationship Existential restriction modifier
Congenital oculocutaneous hypopigmentation Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 3
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 4
Congenital oculocutaneous hypopigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Congenital oculocutaneous hypopigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier 4
Congenital oculocutaneous hypopigmentation Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital oculocutaneous hypopigmentation Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 1
Congenital oculocutaneous hypopigmentation Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Vici syndrome Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier
Osteoporosis and oculocutaneous hypopigmentation syndrome Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier
Ocular albinism with congenital sensorineural deafness Is a False Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier
Waardenburg syndrome type 1 Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier
Waardenburg syndrome type 2 Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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