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789160000: Focal facial dermal dysplasia type III (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3787385018 Setleis syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787386017 Focal facial dermal dysplasia 3 Setleis type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3787387014 Focal facial dermal dysplasia type III en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3787388016 Focal facial dermal dysplasia type III (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3787389012 FFDD type 3 - focal facial dermal dysplasia type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787390015 Focal facial dermal dysplasia type III (FFDD3) is a rare focal facial dermal dysplasia with primary characteristics of congenital bitemporal scar-like depressions and a typical but variable facial dysmorphism. Caused by homozygous mutations in the TWIST2 gene, which encodes a bHLH transcription factor involved in dermal facial development in mammals. However, the majority of unrelated FFDD3 patients evaluated have had normal TWIST2 sequences, indicating the molecular genetic heterogeneity of the disorder. Many cases are sporadic. Inheritance is autosomal recessive for patients with TWIST2 mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787385018 Setleis syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787386017 Focal facial dermal dysplasia 3 Setleis type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3787387014 Focal facial dermal dysplasia type III en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3787388016 Focal facial dermal dysplasia type III (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3787389012 FFDD type 3 - focal facial dermal dysplasia type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3787390015 Focal facial dermal dysplasia type III (FFDD3) is a rare focal facial dermal dysplasia with primary characteristics of congenital bitemporal scar-like depressions and a typical but variable facial dysmorphism. Caused by homozygous mutations in the TWIST2 gene, which encodes a bHLH transcription factor involved in dermal facial development in mammals. However, the majority of unrelated FFDD3 patients evaluated have had normal TWIST2 sequences, indicating the molecular genetic heterogeneity of the disorder. Many cases are sporadic. Inheritance is autosomal recessive for patients with TWIST2 mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
6158291000241118 dysplasie dermique focale de la face, type III fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6158301000241119 dysplasie dermique focale du visage, type III fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6158291000241118 dysplasie dermique focale de la face, type III fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6158301000241119 dysplasie dermique focale du visage, type III fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Focal facial dermal dysplasia type III (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal facial dermal dysplasia type III (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Focal facial dermal dysplasia type III (disorder) Finding site Ectoderm structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal facial dermal dysplasia type III (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Focal facial dermal dysplasia type III (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Focal facial dermal dysplasia type III (disorder) Is a Focal facial dermal dysplasia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Focal facial dermal dysplasia type III (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Focal facial dermal dysplasia type III (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Focal facial dermal dysplasia type III (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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