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718222000: Autosomal dominant popliteal pterygium syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3311572010 Autosomal dominant popliteal pterygium syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311573017 Autosomal dominant popliteal pterygium syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311574011 Facio-genito-popliteal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311575012 Popliteal web syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311576013 A rare genetic malformation disorder with characteristics of cleft lip, with or without cleft palate, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. Associated with mutations in the IRF6 gene (1q32.2-q32.3) which is involved in the formation of connective and epithelial tissues. Follows an autosomal dominant pattern of inheritance. 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 popliteal pterygium syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant popliteal pterygium syndrome (disorder) Is a Popliteal pterygium syndrome true Inferred relationship Some
Autosomal dominant popliteal pterygium syndrome (disorder) Associated morphology Congenital webbing true Inferred relationship Some 1
Autosomal dominant popliteal pterygium syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant popliteal pterygium syndrome (disorder) Finding site Popliteal region structure true Inferred relationship Some 1
Autosomal dominant popliteal pterygium syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant popliteal pterygium syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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