Mitochondria Phenome Knowledgebase

Phenotypic Feature Aphasia finds 2 Gene-Feature associations that are associated with 2 Genes

Gene OMIM Disease Phenotypic Feature Phenotype Annotation Clinical Category PMIDs
ABCD1 300100 Aphasia neurologic 11204280
ATP7B 277900 Aphasia dysphasia; agraphia neurologic 10864623 12376745 15909172

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