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78642008: Ocular albinism, type I (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1234278016 OA1 - X-linked ocular albinism en Synonym Active Case sensitive SNOMED CT core
1234279012 X-linked ocular albinism en Synonym Active Case sensitive SNOMED CT core
1234280010 X-linked recessive ocular albinism en Synonym Active Case sensitive SNOMED CT core
130493018 X-linked ocular albinism, Nettleship type en Synonym Active Case sensitive SNOMED CT core
200741016 Nettleship-Falls type ocular albinism en Synonym Active Case sensitive SNOMED CT core
200742011 Ocular albinism, type I en Synonym Active Initial character case insensitive SNOMED CT core
3037049018 X linked ocular albinism en Synonym Active Case sensitive SNOMED CT core
819605018 Ocular albinism, type I (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ocular albinism, type I Pathological process Pathological developmental process true Inferred relationship Some 1
Ocular albinism, type I Occurrence Congenital true Inferred relationship Some 1
Ocular albinism, type I Is a X-linked recessive hereditary disease true Inferred relationship Some
Ocular albinism, type I Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Ocular albinism, type I Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
Ocular albinism, type I Is a X-linked hereditary disease false Inferred relationship Some
Ocular albinism, type I Is a Ocular albinism true Inferred relationship Some
Ocular albinism, type I Finding site Eye structure true Inferred relationship Some 1
Ocular albinism, type I Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Ocular albinism, type I Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Ocular albinism, type I Occurrence Congenital false Inferred relationship Some 2
Ocular albinism, type I Occurrence Congenital false Inferred relationship Some 3
Ocular albinism, type I Associated morphology Decreased melanin pigmentation false Inferred relationship Some 2
Ocular albinism, type I Associated morphology Congenital hypopigmentation false Inferred relationship Some 3
Ocular albinism, type I Finding site Skin structure false Inferred relationship Some 3
Ocular albinism, type I Finding site Orbital region structure false Inferred relationship Some 1
Ocular albinism, type I Finding site Structure of skin region false Inferred relationship Some 2
Ocular albinism, type I Associated morphology Congenital anomaly false Inferred relationship Some 1
Ocular albinism, type I Finding site Structure of nervous system false Inferred relationship Some
Ocular albinism, type I Finding site Eye structure false Inferred relationship Some 1
Ocular albinism, type I Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Ocular albinism, type I Associated morphology Congenital deficiency false Inferred relationship Some
Ocular albinism, type I Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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