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35031005: Hanhart's 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
58452016 Hanhart's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
58453014 Micrognathia with peromelia en Synonym Active Entire term case insensitive SNOMED CT core module
766625015 Hanhart's syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2840245012 Hanhart 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
Hanhart's syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Hanhart's syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Hanhart's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Hanhart's syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Hanhart's syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Hanhart's syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Hanhart's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Hanhart's syndrome Associated morphology Morphologically abnormal structure 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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