Other specified congenital musculoskeletal deformities

Preferred Label : Other specified congenital musculoskeletal deformities;

Inclusion CIM-10 : Congenital deformity of clavicle; Congenital deformity of forearm; Congenital dislocation of wrist; Congenital deformity of wrist; Congenital dislocation of elbow; Congenital deformity of scapula; Congenital dislocation of shoulder; Congenital deformity of elbow;

Diag associé à un acte (%) : 95.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q688;

UMLS CUI

C0478066;

Automatic exact mappings (from CISMeF team)
- Congenital deformity of clavicle [MedDRA Preferred Term]
- Congenital deformity of clavicle (disorder) [SNOMED CT concept]
- Congenital deformity of scapula (disorder) [SNOMED CT concept]
- Congenital elbow dislocation [ICD-11 Category]
- Congenital shoulder dislocation [ICD-11 Category]
Currated CISMeF NLP mapping
- Congenital dislocation of elbow (disorder) [SNOMED CT concept]
- Congenital dislocation of shoulder (disorder) [SNOMED CT concept]
- Isolated congenital radial head dislocation [ORDO Disease]
- True congenital shoulder dislocation [ORDO Disease]
- congenital dislocation of elbow [SNOMED Notion]
- congenital dislocation of shoulder [SNOMED Notion]
DO Cross reference
- lethal congenital contracture syndrome [DO Concept]
Orphanet concepts
- Arthrogryposis syndrome [ORDO Disease]
- Arthrogryposis-anterior horn cell disease syndrome [ORDO Disease]
- Arthrogryposis-like hand anomaly-sensorineural deafness syndrome [ORDO Disease]
- Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome [ORDO Disease]
- Arthrogryposis-severe scoliosis syndrome [ORDO Disease]
- Carney complex-trismus-pseudocamptodactyly syndrome [ORDO Disease]
- Congenital bowing of long bones-short stature-dolichomacrocephaly-ocular hypertelorism syndrome [ORDO Disease]
- Congenital contractural arachnodactyly [ORDO Disease]
- Congenital elbow dislocation, bilateral [ORDO Disease]
- Congenital elbow dislocation, unilateral [ORDO Disease]
- Congenitally short costocoracoid ligament [ORDO Disease]
- Distal arthrogryposis [ORDO Disease]
- Distal arthrogryposis type 1 [ORDO Disease]
- Distal arthrogryposis type 10 [ORDO Disease]
- Distal arthrogryposis type 5D [ORDO Disease]
- Gordon syndrome [ORDO Disease]
- Hypomyelination neuropathy-arthrogryposis syndrome [ORDO Disease]
- Isolated congenital radial head dislocation [ORDO Disease]
- Leri pleonosteosis [ORDO Disease]
- Lethal congenital contracture syndrome [ORDO Disease]
- Lethal congenital contracture syndrome type 1 [ORDO Disease]
- Lethal congenital contracture syndrome type 2 [ORDO Disease]
- Lethal congenital contracture syndrome type 3 [ORDO Disease]
- MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome [ORDO Disease]
- Pelvic dysplasia-arthrogryposis of lower limbs syndrome [ORDO Disease]
- Sheldon-Hall syndrome [ORDO Disease]
- Trismus-pseudocamptodactyly syndrome [ORDO Disease]
- True congenital shoulder dislocation [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
Validated automatic mappings to BTNT
- lethal congenital contracture syndrome [DO Concept]

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