Amyotrophy, monomelic

Preferred Label : Amyotrophy, monomelic;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Spinal muscular atrophy, juvenile, nonprogressive; Hirayama disease;

Description : Monomelic amyotrophy, also known as Hirayama disease, is characterized by insidious onset of weakness and wasting of the muscles of the hand and forearm. It is usually unilateral, but can be bilateral. It occurs most commonly as a sporadic condition, is most common in young men, and follows a relatively benign course after a few years of progression (Nalini et al., 2004; Misra et al., 2005).;

Inheritance : Isolated cases;

Prefixed ID : %602440;

Details

Origin ID

602440;

UMLS CUI

C1865384;

Automatic exact mappings (from CISMeF team)
- Monomelic amyotrophy [ICD-11 Subcategory]
- Monomelic amyotrophy of upper limb [ICD-11 More detail]
Currated CISMeF NLP mapping
- Amyotrophy, monomelic [MeSH concept]
- Monomelic amyotrophy [MedDRA Preferred Term]
- Monomelic amyotrophy [ORDO Disease]
- amyotrophy, monomelic [MeSH Supplementary Concept]
HPO term(s)
- Cervical spinal cord atrophy [HPO term]
- Cold paresis [HPO term]
- EMG: neuropathic changes [HPO term]
- Fasciculations [HPO term]
- Insidious onset [HPO term]
- Interosseus muscle atrophy [HPO term]
- Isolated cases [HPO term]
- Sporadic [HPO term]
- Upper limb muscle weakness [HPO term]
ORDO concept(s)
- Monomelic amyotrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyotrophy, monomelic [MeSH concept]
- Monomelic amyotrophy [MedDRA Preferred Term]
- Monomelic amyotrophy [ORDO Disease]
- amyotrophy, monomelic [MeSH Supplementary Concept]

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