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43929004: Smith-Lemli-Opitz syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
73253014 Smith-Lemli-Opitz syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
493717019 7-Dehydrocholesterol reductase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
780998012 Smith-Lemli-Opitz syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Smith-Lemli-Opitz syndrome Is a Multiple malformation syndrome, moderate short stature, facial true Inferred relationship Some
Smith-Lemli-Opitz syndrome Is a Disorder of cholesterol synthesis true Inferred relationship Some
Smith-Lemli-Opitz syndrome Occurrence Congenital false Inferred relationship Some
Smith-Lemli-Opitz syndrome Finding site Body system structure false Inferred relationship Some
Smith-Lemli-Opitz syndrome Associated morphology Congenital malformation false Inferred relationship Some
Smith-Lemli-Opitz syndrome Occurrence Congenital true Inferred relationship Some 1
Smith-Lemli-Opitz syndrome Associated morphology Developmental anomaly false Inferred relationship Some 1
Smith-Lemli-Opitz syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Smith-Lemli-Opitz syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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