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774212003: Microcornea, myopic chorioretinal atrophy, telecanthus syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3728383019 Microcornea, myopic chorioretinal atrophy, telecanthus syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3728384013 MMCAT syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3728385014 MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3728386010 Microcornea, myopic chorioretinal atrophy, telecanthus 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
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Finding site Corneal structure true Inferred relationship Existential restriction modifier 1
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 1
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Finding site Choroidal structure true Inferred relationship Existential restriction modifier 3
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Associated morphology Atrophy true Inferred relationship Existential restriction modifier 2
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Associated morphology Atrophy true Inferred relationship Existential restriction modifier 3
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Is a Chorioretinal atrophy true Inferred relationship Existential restriction modifier
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 2
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Is a Congenital malformation syndrome true Inferred relationship Existential restriction modifier
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Is a Microcornea true Inferred relationship Existential restriction modifier
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome 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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