cardiomyopathy, dilated, 1M; CMD1M
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http://purl.obolibrary.org/obo/MONDO_0011840 |
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CSRP3 familial isolated dilated cardiomyopathy
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http://purl.obolibrary.org/obo/MONDO_0011840 |
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biotin-responsive basal ganglia disease
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http://purl.obolibrary.org/obo/MONDO_0011841 |
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thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive type)
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http://purl.obolibrary.org/obo/MONDO_0011841 |
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thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive type); THMD2
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http://purl.obolibrary.org/obo/MONDO_0011841 |
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biotin-thiamine-responsive basal ganglia disease
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http://purl.obolibrary.org/obo/MONDO_0011841 |
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encephalopathy, thiamine-responsive
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http://purl.obolibrary.org/obo/MONDO_0011841 |
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basal ganglia disease, biotin-responsive
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http://purl.obolibrary.org/obo/MONDO_0011841 |
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Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
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http://purl.obolibrary.org/obo/MONDO_0011842 |
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dementia, hereditary dysphasic disinhibition
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http://purl.obolibrary.org/obo/MONDO_0011842 |
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frontotemporal lobar degeneration with Tdp43 inclusions, Grn-related
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http://purl.obolibrary.org/obo/MONDO_0011842 |
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frontotemporal lobar Degeneration with ubiquitin-positive inclusions
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http://purl.obolibrary.org/obo/MONDO_0011842 |
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