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890233009: Autosomal dominant Robinow syndrome (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4011661016 Autosomal dominant Robinow syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4011663018 Autosomal dominant Robinow syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant Robinow syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant Robinow syndrome Is a Robinow syndrome true Inferred relationship Existential restriction modifier
Autosomal dominant Robinow syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier 1
Autosomal dominant Robinow syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Autosomal dominant Robinow syndrome Finding site Skeletal system structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant Robinow syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Autosomal dominant Robinow syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Autosomal dominant Robinow syndrome Finding site Musculoskeletal structure of limb true Inferred relationship Existential restriction modifier 3
Autosomal dominant Robinow syndrome Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier 3
Autosomal dominant Robinow syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Autosomal dominant Robinow syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Autosomal dominant Robinow syndrome Finding site Bone structure of spine true Inferred relationship Existential restriction modifier 4
Autosomal dominant Robinow syndrome Associated morphology Aplasia true Inferred relationship Existential restriction modifier 4
Autosomal dominant Robinow syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Autosomal dominant Robinow syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Autosomal dominant Robinow syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Autosomal dominant Robinow syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 5
Autosomal dominant Robinow syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 5
Autosomal dominant Robinow syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 5
Autosomal dominant Robinow syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 6

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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