Other congenital malformations of musculoskeletal system

Preferred Label : Other congenital malformations of musculoskeletal system;

Inclusion CIM-10 : Congenital shortening of tendon; Poland syndrome; Amyotrophia congenita; Accessory muscle; Congenital constricting bands; Absence of tendon; Absence of muscle;

Diag associé à un acte (%) : 94.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q798;

UMLS CUI

C0478080;

Automatic exact mappings (from CISMeF team)
- Accessory muscle [MedDRA Preferred Term]
- Accessory skeletal muscle (disorder) [SNOMED CT concept]
- Amyotrophia congenita (disorder) [SNOMED CT concept]
- Congenital shortening of tendon (disorder) [SNOMED CT concept]
- Constricting bands, congenital [OMIM Phenotype]
- Constriction ring syndrome (disorder) [SNOMED CT concept]
- Poland Syndrome [NCIt concept]
- Poland anomaly (disorder) [SNOMED CT concept]
- Poland syndrome [ORDO Disease]
- Poland syndrome [DO Concept]
- Poland syndrome [ICD-11 Sub-sub category]
- Poland syndrome [OMIM Phenotype]
- Poland syndrome [PASCAL descriptor]
- Poland's syndrome [MedDRA Preferred Term]
- Syndrome Polands [MedDRA LLT]
- poland syndrome [MeSH Descriptor]
- poland syndrome [MeSH concept]
DO Cross reference
- Poland syndrome [DO Concept]
Excluded by
- Congenital malformations of breast [ICD-10 category]
Orphanet concepts
- Amniotic bands [ORDO Disease]
- Autosomal dominant multiple pterygium syndrome [ORDO Disease]
- Autosomal recessive multiple pterygium syndrome [ORDO Disease]
- Constriction rings syndrome [ORDO Disease]
- Kyphomelic dysplasia [ORDO Disease]
- Lethal multiple pterygium syndrome [ORDO Disease]
- Multiple pterygium syndrome [ORDO Disease]
- Multiple pterygium syndrome, Aslan type [ORDO Disease]
- Ossification anomalies-psychomotor developmental delay syndrome [ORDO Disease]
- Poland syndrome [ORDO Disease]
- Terminal transverse defects of arm [ORDO Disease]
- X-linked lethal multiple pterygium syndrome [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Other and unspecified anomalies of musculoskeletal system [ICD-9 code]
Validated automatic mappings to BTNT
- Acromelic dysplasias [ICD-11 Subcategory]
- Acromesomelic dysplasias [ICD-11 Subcategory]
- Apert syndrome [ICD-11 Sub-sub category]
- Langer-Giedion syndrome [ICD-11 Sub-sub category]
- Mesomelic or rhizomesomelic dysplasias [ICD-11 Subcategory]

Keyword's position in hierarchy(ies) :

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