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703539006: Manitoba oculotrichoanal syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3008869012 Manitoba oculotrichoanal syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3008917018 MOTA - Manitoba oculotrichoanal syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3009421010 Marles-Greenburg-Persaud syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3009686012 Manitoba oculotrichoanal syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3009696015 Marles syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Manitoba oculotrichoanal syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Manitoba oculotrichoanal syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Manitoba oculotrichoanal syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Manitoba oculotrichoanal syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Manitoba oculotrichoanal syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Manitoba oculotrichoanal syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Manitoba oculotrichoanal 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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