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766765009: syndrome radio-rénal (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1018851000172116 syndrome radio-rénal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3662547018 Radio-renal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3662548011 Radio-renal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768381000241114 syndrome radio-rénal (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3662549015 A rare developmental defect during embryogenesis with characteristics of variable upper limb reduction defects and renal anomalies. Patients typically present absence/hypoplasia of digits, radii and/or ulnae, short stature and mild external ear malformation, as well as kidney agenesis or ectopia. There have been no further descriptions in the literature since 1983. 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
syndrome radio-rénal Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
syndrome radio-rénal est un(e) (attribut) Congenital anomaly of limb false Inferred relationship Some
syndrome radio-rénal Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
syndrome radio-rénal morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
syndrome radio-rénal est un(e) (attribut) anomalie morphologique congénitale false Inferred relationship Some
syndrome radio-rénal est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
syndrome radio-rénal est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
syndrome radio-rénal survenue (attribut) congénital true Inferred relationship Some 1
syndrome radio-rénal est un(e) (attribut) Longitudinal deficiency of limb true Inferred relationship Some
syndrome radio-rénal est un(e) (attribut) anomalie congénitale des reins true Inferred relationship Some
syndrome radio-rénal est un(e) (attribut) Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
syndrome radio-rénal est un(e) (attribut) Hereditary nephropathy (disorder) true Inferred relationship Some
syndrome radio-rénal survenue (attribut) congénital true Inferred relationship Some 2
syndrome radio-rénal localisation d'une constatation (attribut) Entire limb true Inferred relationship Some 1
syndrome radio-rénal morphologie associée (attribut) Abnormal shortening true Inferred relationship Some 1
syndrome radio-rénal morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
syndrome radio-rénal localisation d'une constatation (attribut) structure d'un rein true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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