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61649007: Congenital oculocutaneous hypopigmentation (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
102437010 Congenital oculocutaneous hypopigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
800734016 Congenital oculocutaneous hypopigmentation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
102437010 Congenital oculocutaneous hypopigmentation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
102437010 Congenital oculocutaneous hypopigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
800734016 Congenital oculocutaneous hypopigmentation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
800734016 Congenital oculocutaneous hypopigmentation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
646051000274119 Kongenitale okulokutane Hypomelanose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
646061000274116 Kongenitale okulokutane Hypopigmentierung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5820231000241112 hypopigmentation congénitale des yeux et de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5820241000241119 hypopigmentation oculocutanée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5820231000241112 hypopigmentation congénitale des yeux et de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5820241000241119 hypopigmentation oculocutanée congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
646051000274119 Kongenitale okulokutane Hypomelanose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
646061000274116 Kongenitale okulokutane Hypopigmentierung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


24 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 (core metadata concept)
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of eye true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Finding site Eye structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Is a Disorder of eye region false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Is a Ear, face and neck congenital anomalies (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of skin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Is a Skin lesion false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Is a Congenital deficiency of pigment of skin true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital oculocutaneous hypopigmentation Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital oculocutaneous hypopigmentation Finding site Integumentary system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital oculocutaneous hypopigmentation Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Is a Skin hypopigmented false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital oculocutaneous hypopigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital oculocutaneous hypopigmentation Is a Lesion of eye (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculocutaneous hypopigmentation Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital oculocutaneous hypopigmentation Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital oculocutaneous hypopigmentation Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital oculocutaneous hypopigmentation Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital oculocutaneous hypopigmentation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital oculocutaneous hypopigmentation Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital oculocutaneous hypopigmentation Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Vici syndrome (disorder) Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
Oculocutaneous albinism Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
Okulärer Albinismus mit kongenitaler sensorineuraler Schwerhörigkeit Is a False Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
Waardenburg syndrome type 1 (disorder) Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)
Waardenburg syndrome type 2 (disorder) Is a True Congenital oculocutaneous hypopigmentation Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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