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8757006: Hecht 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
15445015 Hecht syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
15446019 Trismus pseudocamptodactyly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
830072015 Hecht 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
Hecht syndrome Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings true Inferred relationship Existential restriction modifier
Hecht syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Hecht syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 1
Hecht syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Hecht syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hecht syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Hecht syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Hecht syndrome Pathological process Pathological developmental process 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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