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363045008: Connective tissue hereditary disorder (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3038367019 Inherited disorder of connective tissue en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
482180014 Connective tissue hereditary disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
754824015 Connective tissue hereditary disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

142 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Connective tissue hereditary disorder est un(e) (attribut) affection du tissu conjonctif true Inferred relationship Some
Connective tissue hereditary disorder est un(e) (attribut) Hereditary disorder by system false Inferred relationship Some
Connective tissue hereditary disorder localisation d'une constatation (attribut) Connective tissue structure true Inferred relationship Some 1
Connective tissue hereditary disorder localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Connective tissue hereditary disorder est un(e) (attribut) maladie héréditaire false Inferred relationship Some
Connective tissue hereditary disorder est un(e) (attribut) maladie héréditaire true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
epidermolyse bulleuse dystrophique dominante acrale est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
SCARF syndrome est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Vitamin D-dependent rickets est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Goldenhar syndrome est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Autosomal dominant tubulointerstitial disease (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Connective tissue disorder due to lysyl hydroxylase-3 deficiency est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Cerebrofacioarticular syndrome (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Velofacioskeletal syndrome (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
syndrome de mèches blanches et anomalies multiples est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
syndrome de Larsen-like de type B3GAT3 (beta-1,3 glucuronyltransferase 3) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Keipert syndrome (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Spondyloperipheral dysplasia (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Spondyloepimetaphyseal dysplasia Handigodu type est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Spondyloepimetaphyseal dysplasia anauxetic type (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
dysplasie dyssegmentaire type Silverman-Handmaker est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Cono-spondylar dysplasia (disorder) est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
dysplasie spondylo-épimétaphysaire avec luxations multiples est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (disorder) est un(e) (attribut) True Connective tissue hereditary disorder Inferred relationship Some
Multicentric carpotarsal osteolysis syndrome est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Otopalatodigital syndrome est un(e) (attribut) False Connective tissue hereditary disorder Inferred relationship Some
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome (disorder) est un(e) (attribut) True Connective tissue hereditary disorder Inferred relationship Some

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