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

715632003: Oculocutaneous albinism type 4 (disorder)


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
5400998010 A form of oculocutaneous albinism characterized by varying degrees of skin and hair hypopigmentation, numerous ocular changes and misrouting of the optic nerves at the chiasm. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400999019 A form of oculocutaneous albinism characterised by varying degrees of skin and hair hypopigmentation, numerous ocular changes and misrouting of the optic nerves at the chiasm. 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) Is a Oculocutaneous albinism true Inferred relationship Some
Oculocutaneous albinism type 4 (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Oculocutaneous albinism type 4 (disorder) Associated morphology Decreased melanin pigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) Associated morphology Congenital hypopigmentation false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) Finding site Skin structure false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) Finding site Eye structure false Inferred relationship Some 4
Oculocutaneous albinism type 4 (disorder) Associated morphology Decreased melanin pigmentation false Inferred relationship Some 5
Oculocutaneous albinism type 4 (disorder) Occurrence Congenital false Inferred relationship Some 5
Oculocutaneous albinism type 4 (disorder) Associated morphology Congenital hypopigmentation false Inferred relationship Some 6
Oculocutaneous albinism type 4 (disorder) Occurrence Congenital false Inferred relationship Some 6
Oculocutaneous albinism type 4 (disorder) Finding site Skin structure false Inferred relationship Some 6
Oculocutaneous albinism type 4 (disorder) Occurrence Congenital true Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) Finding site Eye structure true Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) Finding site Eye structure false Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) Occurrence Congenital true Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) Finding site Skin structure 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) Finding site Skin structure false Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) Associated morphology Hypopigmentation false Inferred relationship Some 1
Oculocutaneous albinism type 4 (disorder) Associated morphology Hypopigmentation false Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) Associated morphology Decreased melanin pigmentation true Inferred relationship Some 2
Oculocutaneous albinism type 4 (disorder) Associated morphology Decreased melanin pigmentation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start