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14921002: Aarskog syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
25344018 Aarskog syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
741421011 Aarskog syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aarskog syndrome Is a Multiple malformation syndrome, moderate short stature, facial true Inferred relationship Existential restriction modifier
Aarskog syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Aarskog syndrome Is a Congenital malformation syndromes associated with short stature true Inferred relationship Existential restriction modifier
Aarskog syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Aarskog syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Aarskog syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Aarskog syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Aarskog syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Aarskog syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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