FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

63450009: Rufous albinism (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
105470011 Rufous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
105471010 Red-skin albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499595015 Rufous oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
802734013 Rufous albinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2536411012 Xanthism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Rufous albinism Is a Tyrosinase-positive oculocutaneous albinism true Inferred relationship Some
Rufous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Rufous albinism Finding site Skin structure false Inferred relationship Some 3
Rufous albinism Finding site Structure of skin region false Inferred relationship Some 1
Rufous albinism Associated morphology Congenital deficiency false Inferred relationship Some
Rufous albinism Finding site Eye structure false Inferred relationship Some 1
Rufous albinism Occurrence Congenital false Inferred relationship Some
Rufous albinism Associated morphology Red color false Inferred relationship Some
Rufous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Rufous albinism Finding site Skin structure false Inferred relationship Some 1
Rufous albinism Due to Disorder of tyrosine metabolism false Inferred relationship Some
Rufous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
Rufous albinism Finding site Eye structure false Inferred relationship Some 1
Rufous albinism Finding site Skin structure true Inferred relationship Some 1
Rufous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Rufous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1
Rufous albinism Occurrence Congenital true Inferred relationship Some 2
Rufous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Some 2
Rufous albinism Finding site Skin structure false Inferred relationship Some 2
Rufous albinism Occurrence Congenital false Inferred relationship Some 3
Rufous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
Rufous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Some 2
Rufous albinism Occurrence Congenital true Inferred relationship Some 1
Rufous albinism Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Rufous albinism Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Rufous albinism Finding site Eye structure true Inferred relationship Some 2
Rufous albinism Associated morphology Hypopigmentation false Inferred relationship Some 2
Rufous albinism Associated morphology Hypopigmentation false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start