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722060007: Oculogastrointestinal muscular dystrophy (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
3330422010 Oculogastrointestinal muscular dystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330423017 Oculogastrointestinal muscular dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
3330424011 Visceral myopathy with familial external ophthalmoplegia 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
Oculogastrointestinal muscular dystrophy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Oculogastrointestinal muscular dystrophy Is a Congenital anomaly of visual system true Inferred relationship Existential restriction modifier
Oculogastrointestinal muscular dystrophy Is a Motility disorder of intestine false Inferred relationship Existential restriction modifier
Oculogastrointestinal muscular dystrophy Is a Pseudo-obstruction of intestine true Inferred relationship Existential restriction modifier
Oculogastrointestinal muscular dystrophy Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Oculogastrointestinal muscular dystrophy Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Oculogastrointestinal muscular dystrophy Associated morphology Pseudo-obstruction true Inferred relationship Existential restriction modifier 2
Oculogastrointestinal muscular dystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Oculogastrointestinal muscular dystrophy Finding site Intestinal structure true Inferred relationship Existential restriction modifier 2
Oculogastrointestinal muscular dystrophy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Oculogastrointestinal muscular dystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Oculogastrointestinal muscular dystrophy Finding site Structure of visual system false Inferred relationship Existential restriction modifier 3
Oculogastrointestinal muscular dystrophy Is a Congenital anomaly of intestinal tract true Inferred relationship Existential restriction modifier
Oculogastrointestinal muscular dystrophy Finding site Structure of visual system true Inferred relationship Existential restriction modifier 1
Oculogastrointestinal muscular dystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Oculogastrointestinal muscular dystrophy Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Oculogastrointestinal muscular dystrophy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Oculogastrointestinal muscular dystrophy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Oculogastrointestinal muscular dystrophy Is a Developmental hereditary disorder 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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