FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

26336006: Tyrosinase-positive oculocutaneous 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
1225002010 OCA2 - Tyrosinase-positive oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3758343013 Albinoidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3758345018 Oculocutaneous albinism type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
410611000241117 albinisme oculo-cutané type 2 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
44104018 Tyrosinase-positive oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
50012531000188111 albinisme oculo-cutané type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
50012541000188116 AOC2 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
50012551000188119 albinisme oculo-cutané tyrosinase-positive fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
756757013 Tyrosinase-positive oculocutaneous albinism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) Structure of eye proper (body structure) true Inferred relationship Some 2
albinisme oculo-cutané type 2 (trouble) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 2
albinisme oculo-cutané type 2 (trouble) est un(e) (attribut) Oculocutaneous albinism true Inferred relationship Some
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) Due to Disorder of tyrosine metabolism (disorder) false Inferred relationship Some
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3
albinisme oculo-cutané type 2 (trouble) survenue (attribut) congénital true Inferred relationship Some 2
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 2
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
albinisme oculo-cutané type 2 (trouble) survenue (attribut) congénital false Inferred relationship Some 3
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 3
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 2
albinisme oculo-cutané type 2 (trouble) survenue (attribut) congénital false Inferred relationship Some
albinisme oculo-cutané type 2 (trouble) morphologie associée (attribut) Congenital deficiency false Inferred relationship Some
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) Structure of skin region false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 1
albinisme oculo-cutané type 2 (trouble) survenue (attribut) congénital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Punctate oculocutaneous albinoidism est un(e) (attribut) True albinisme oculo-cutané type 2 (trouble) Inferred relationship Some
Cross syndrome est un(e) (attribut) False albinisme oculo-cutané type 2 (trouble) Inferred relationship Some
Rufous albinism est un(e) (attribut) True albinisme oculo-cutané type 2 (trouble) Inferred relationship Some
Hermansky-Pudlak syndrome est un(e) (attribut) True albinisme oculo-cutané type 2 (trouble) Inferred relationship Some
Chédiak-Higashi syndrome est un(e) (attribut) False albinisme oculo-cutané type 2 (trouble) Inferred relationship Some
Brown oculocutaneous albinism est un(e) (attribut) True albinisme oculo-cutané type 2 (trouble) Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Back to Start