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703539006: Manitoba oculotrichoanal syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3008869012 Manitoba oculotrichoanal syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3008917018 MOTA - Manitoba oculotrichoanal syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009421010 Marles-Greenburg-Persaud syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009686012 Manitoba oculotrichoanal syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009696015 Marles syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6335981000241110 syndrome de Marles fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6335991000241112 syndrome MOTA (manitoba-oculo-tricho-anal) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6336001000241111 syndrome oculo-tricho-anal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3389801001000116 Okulo-tricho-anales Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 Some
Manitoba oculotrichoanal syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Manitoba oculotrichoanal syndrome Occurrence Congenital true Inferred relationship Some 1
Manitoba oculotrichoanal syndrome Associated morphology anomalie du développement false Inferred relationship Some 1
Manitoba oculotrichoanal syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Manitoba oculotrichoanal syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Manitoba oculotrichoanal syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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