Muscular dystrophy, progressive pectorodorsal

Preferred Label : Muscular dystrophy, progressive pectorodorsal;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Muscular dystrophy, progressive, involving shoulder girdle and back;

Inheritance : X-linked;

Prefixed ID : 310095;

Details

Origin ID

310095;

UMLS CUI

C1839669;

Currated CISMeF NLP mapping
- muscular dystrophy, progressive pectorodorsal [MeSH concept]
- muscular dystrophy, progressive pectorodorsal [MeSH Supplementary Concept]
DO Cross reference
- muscular dystrophy [DO Concept]
HPO term(s)
- Abnormality of cardiac conduction [HPO term]
- Arrhythmia [HPO term]
- Elevated circulating creatine kinase concentration [HPO term]
- Muscular dystrophy [HPO term]
- Scapular winging [HPO term]
- Shoulder girdle muscle weakness [HPO term]
- X-linked inheritance [HPO term]
Not associated HPO term(s)
- Facial palsy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- muscular dystrophy, progressive pectorodorsal [MeSH Supplementary Concept]
- muscular dystrophy, progressive pectorodorsal [MeSH concept]
Validated automatic mappings to NTBT
- muscular dystrophy [DO Concept]

Keyword's position in hierarchy(ies) :

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