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700211007: Ulnar mammary 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
2989585014 Ulnar mammary syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2989606017 Ulnar mammary syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2989640017 Ulnar-mammary syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2989657018 Schinzel 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
Ulnar mammary syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Ulnar mammary syndrome Is a Anomaly of chromosome pair 12 true Inferred relationship Existential restriction modifier
Ulnar mammary syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ulnar mammary syndrome Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Ulnar mammary syndrome Finding site Chromosome pair 12 true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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