| Metadata | |
|---|---|
| ID | DOID:0080102 |
| Name | congenital myopathy 4A |
| Definition | A congenital myopathy that is characterized by skeletal muscle weakness, particularly in the muscles of the shoulders, upper arms, hips, and thighs. https://ghr.nlm.nih.gov/condition/congenital-fiber-type-disproportion |
| Xrefs | |
| Synonyms |
CFTD [EXACT] congenital fiber-type disproportion [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a congenital myopathy is_a physical disorder |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance disease has basis in some Abnormality of prenatal development or birth |