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890233009: Autosomal dominant Robinow syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4011661016 Autosomal dominant Robinow syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4011663018 Autosomal dominant Robinow syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4011662011 The more common type of Robinow syndrome characterized by mild to moderate limb shortening and abnormalities of the head, face and external genitalia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4011664012 The more common type of Robinow syndrome characterised by mild to moderate limb shortening and abnormalities of the head, face and external genitalia. en Definition 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
Autosomal dominant Robinow syndrome (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant Robinow syndrome (disorder) est un(e) (attribut) Robinow syndrome true Inferred relationship Some
Autosomal dominant Robinow syndrome (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 1
Autosomal dominant Robinow syndrome (disorder) morphologie associée (attribut) dysplasie true Inferred relationship Some 2
Autosomal dominant Robinow syndrome (disorder) localisation d'une constatation (attribut) Skeletal system structure true Inferred relationship Some 2
Autosomal dominant Robinow syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Autosomal dominant Robinow syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Autosomal dominant Robinow syndrome (disorder) localisation d'une constatation (attribut) Musculoskeletal structure of limb true Inferred relationship Some 3
Autosomal dominant Robinow syndrome (disorder) morphologie associée (attribut) Abnormally short growth true Inferred relationship Some 3
Autosomal dominant Robinow syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Autosomal dominant Robinow syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Autosomal dominant Robinow syndrome (disorder) localisation d'une constatation (attribut) structure osseuse de la colonne vertébrale (structure corporelle) true Inferred relationship Some 4
Autosomal dominant Robinow syndrome (disorder) morphologie associée (attribut) Aplasia true Inferred relationship Some 4
Autosomal dominant Robinow syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 4
Autosomal dominant Robinow syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Autosomal dominant Robinow syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 5
Autosomal dominant Robinow syndrome (disorder) localisation d'une constatation (attribut) face true Inferred relationship Some 5
Autosomal dominant Robinow syndrome (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 5
Autosomal dominant Robinow syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Autosomal dominant Robinow syndrome (disorder) interprète (attribut) Height / growth measure true Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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