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719299009: Pelviscapular dysplasia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3315905012 Pelviscapular dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315906013 Cousin syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315907016 Familial pelvis-scapular dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315909018 Pelviscapular dysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315910011 Pelviscapular dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315908014 Syndrome with characteristics of pelviscapular dysplasia with epiphyseal abnormalities, congenital dwarfism and facial dysmorphism. The facial dysmorphism has manifestations of frontal bossing, hypertelorism, narrow palpebral fissures, deep-set eyes, strabismus, low-set posteriorly rotated and malformed ears, dysplasia of conchae, a small chin, a short neck with redundant skin folds, and a low hairline. Intelligence may vary from normal to moderately impaired. Radiographic features comprise aplasia of the body of the scapula, hypoplasia of the iliac bone, humeroradial synostosis, dislocation of the femoral heads, and moderate brachydactyly. Mutations in the TBX15 gene have been identified as potentially causative. Pelviscapular dysplasia is phenotypically similar to pelvis-shoulder dysplasia. 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
Pelviscapular dysplasia survenue (attribut) congénital true Inferred relationship Some 1
Pelviscapular dysplasia morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
Pelviscapular dysplasia morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Pelviscapular dysplasia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Pelviscapular dysplasia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Pelviscapular dysplasia localisation d'une constatation (attribut) Bone structure of extremity true Inferred relationship Some 1
Pelviscapular dysplasia morphologie associée (attribut) dysplasie true Inferred relationship Some 1
Pelviscapular dysplasia est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Pelviscapular dysplasia est un(e) (attribut) Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Pelviscapular dysplasia est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Pelviscapular dysplasia est un(e) (attribut) Dysostosis true Inferred relationship Some
Pelviscapular dysplasia est un(e) (attribut) Connective tissue hereditary disorder false Inferred relationship Some
Pelviscapular dysplasia est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some
Pelviscapular dysplasia morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Pelviscapular dysplasia survenue (attribut) congénital true Inferred relationship Some 2
Pelviscapular dysplasia localisation d'une constatation (attribut) face true Inferred relationship Some 2
Pelviscapular dysplasia morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 3
Pelviscapular dysplasia survenue (attribut) congénital false Inferred relationship Some 3
Pelviscapular dysplasia localisation d'une constatation (attribut) Bone structure of extremity false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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