OBO ID: DOID:0110638 |
Term Name: | obsolete congenital muscular dystrophy merosin-positive | Search Ontology: | |
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Synonyms: |
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Definition: | A congenital muscular dystrophy characterized by autosomal recessive inheritance of generalized muscle weakness and hypotonia without arthrogryposis or central nervous system involvement that has_material_basis_in mutation in the chromosome region 4p16.3. (3) | ||
References: | |||
Ontology: | Human Disease ( DOID:0110638 ) | ||
Obsolete: | true |
OTHER obsolete congenital muscular dystrophy merosin-positive PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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