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722061006: Oculoosteocutaneous syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3330427016 Oculoosteocutaneous syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330428014 Oculoosteocutaneous syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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