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MCID: CNG549
MIFTS: 9
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Congenital Muscular Dystrophy-Dystroglycanopathy Type A9
Categories:
Eye diseases, Fetal diseases, Genetic diseases, Mental diseases, Metabolic diseases, Muscle diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Congenital Muscular Dystrophy-Dystroglycanopathy Type A9:
Name: Congenital Muscular Dystrophy-Dystroglycanopathy Type A9
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Classifications:
MalaCards categories:
Global: Genetic diseases Rare diseases Metabolic diseases Fetal diseases Anatomical: Muscle diseases Neuronal diseases Eye diseases Mental diseases External Ids:
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Disease Ontology :
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A congenital muscular dystrophy-dystroglycanopathy type A that has material basis in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.
MalaCards based summary : Congenital Muscular Dystrophy-Dystroglycanopathy Type A9, also known as congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type a9, is related to muscular dystrophy-dystroglycanopathy , type a, 9. Affiliated tissues include eye and brain. |
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MalaCards organs/tissues related to Congenital Muscular Dystrophy-Dystroglycanopathy Type A9:40
Eye,
Brain
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Search
GEO
for disease gene expression data for Congenital Muscular Dystrophy-Dystroglycanopathy Type A9.
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