Muscular dystrophy, congenital, producing arthrogryposis

Preferred Label : Muscular dystrophy, congenital, producing arthrogryposis;

Obsolete resource : true;

Moved to : 618484; 619334;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : 253900;

Details

Origin ID

253900;

UMLS CUI

C1850865;

Currated CISMeF NLP mapping
- Arthrogryposis due to muscular dystrophy [ORDO Disease]
- arthrogryposis due to muscular dystrophy [DO Concept]
- muscular dystrophy, congenital, producing arthrogryposis [MeSH concept]
- muscular dystrophy, congenital, producing arthrogryposis [MeSH Supplementary Concept]
DO Cross reference
- arthrogryposis due to muscular dystrophy [DO Concept]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Arthrogryposis multiplex congenita [HPO term]
- Autosomal recessive inheritance [HPO term]
- Congenital muscular dystrophy [HPO term]
- Myopathy [HPO term]
ORDO concept(s)
- Arthrogryposis due to muscular dystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Arthrogryposis due to muscular dystrophy [ORDO Disease]
- arthrogryposis due to muscular dystrophy [DO Concept]
- muscular dystrophy, congenital, producing arthrogryposis [MeSH Supplementary Concept]
- muscular dystrophy, congenital, producing arthrogryposis [MeSH concept]

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