FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

715632003: albinisme oculo-cutané type 4 (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303240010 Oculocutaneous albinism type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303241014 Oculocutaneous albinism type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
748091000241115 albinisme oculo-cutané type 4 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
887181000172119 albinisme oculo-cutané type 4 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
891521000172115 AOC4 - albinisme oculo-cutané type 4 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303242019 A type of Oculocutaneous albinism with varying degrees of skin and hair hypopigmentation, numerous ocular changes and misrouting of the optic nerves at the chiasm. Cutaneous hypopigmentation is often visible at birth and signs of nystagmus and strabismus present in the first year of life. Visual changes are not progressive. Caused by mutations in the membrane-associated transporter protein (MATP) gene, SLC45A2, encoding a transporter protein which is thought to mediate melanin synthesis. Inheritance is autosomal recessive. en Definition 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
Oculocutaneous albinism type 4 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Hypopigmentation false Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Decreased melanin pigmentation true Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) est un(e) (attribut) Oculocutaneous albinism true Inferred relationship Some
Oculocutaneous albinism type 4 (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Decreased melanin pigmentation false Inferred relationship Some 5
Oculocutaneous albinism type 4 (disorder) survenue (attribut) congénital false Inferred relationship Some 5
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 6
Oculocutaneous albinism type 4 (disorder) survenue (attribut) congénital false Inferred relationship Some 6
Oculocutaneous albinism type 4 (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 6
Oculocutaneous albinism type 4 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) true Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) morphologie associée (attribut) Congenital hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) localisation d'une constatation (attribut) Structure of eye proper (body structure) false Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) survenue (attribut) congénital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start