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14921002: Aarskog syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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