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78642008: Ocular albinism, type I (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
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 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 (body structure) 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
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 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 Pathological process (attribute) 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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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