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722061006: Oculoosteocutaneous syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330427016 Oculoosteocutaneous syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3330428014 Oculoosteocutaneous syndrome en Synonym Active Case insensitive SNOMED CT core
3330429018 This syndrome has characteristics of congenital anodontia, a small maxilla, short stature with shortened metacarpals and metatarsals, sparse hair, albinoidism and multiple ocular anomalies. It has been described in three siblings (one brother and two sisters). Transmission is autosomal recessive. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculoosteocutaneous syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Oculoosteocutaneous syndrome Occurrence Congenital true Inferred relationship Some 1
Oculoosteocutaneous syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Oculoosteocutaneous syndrome Finding site Ectoderm structure true Inferred relationship Some 1
Oculoosteocutaneous syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Oculoosteocutaneous syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Oculoosteocutaneous syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Oculoosteocutaneous syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Oculoosteocutaneous syndrome Pathological process Pathological developmental process true Inferred relationship Some 3
Oculoosteocutaneous syndrome Is a Digestive system hereditary disorder false Inferred relationship Some
Oculoosteocutaneous syndrome Finding site Hair structure true Inferred relationship Some 2
Oculoosteocutaneous syndrome Finding site Tooth structure true Inferred relationship Some 3
Oculoosteocutaneous syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Oculoosteocutaneous syndrome Is a Hereditary disorder of tooth true Inferred relationship Some
Oculoosteocutaneous syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Oculoosteocutaneous syndrome Is a Ectodermal dysplasia with hair-tooth defects true Inferred relationship Some
Oculoosteocutaneous syndrome Is a Hereditary disorder of the integument true Inferred relationship Some
Oculoosteocutaneous syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 2
Oculoosteocutaneous syndrome Occurrence Congenital true Inferred relationship Some 2
Oculoosteocutaneous syndrome Finding site Ectoderm structure false Inferred relationship Some 2
Oculoosteocutaneous syndrome Associated morphology Developmental abnormality false Inferred relationship Some 3
Oculoosteocutaneous syndrome Occurrence Congenital true Inferred relationship Some 3
Oculoosteocutaneous syndrome Finding site Skin structure false Inferred relationship Some 3
Oculoosteocutaneous syndrome Finding site Skin structure false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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