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Disease core ontology applied to Rare Diseases
Last uploaded:
February 7, 2014
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Preferred Name | Familial isolated dilated cardiomyopathy | |
Synonyms |
Familial or idiopathic dilated cardiomyopathy |
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ID |
http://www.limics.org/hrdo/rdfns#pat_id_635 |
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ageOfDeath |
Any age
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ageOfOnset |
Variable
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altLabel |
Familial or idiopathic dilated cardiomyopathy
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id_Medline | ||
id_MIM |
302045 600884 601154 601493 601494 604145 604288 604765 605582 606685 607482 607487 608569 609909 609915 611407 611615 611878 611879 611880 612158 612877 613122 613172 613252 613286 613424 613426 613642 613694 613697 613740 613881 614672 615184 615235 615248
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id_OMS |
I42.0
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id_Orpha |
154
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inheritance |
X-linked recessive Autosomal dominant Mitochondrial inheritance Autosomal recessive
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patType |
disease
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prefixIRI |
hrdo:pat_id_635
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prefLabel |
Familial isolated dilated cardiomyopathy
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|
prevalence |
1-5 / 10 000
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subClassOf |
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Mapping To | Ontology | Source |
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http://www.orpha.net/ORDO/Orphanet_154 | ORDO | LOOM |
http://purl.obolibrary.org/obo/MONDO_0015470 | DOVES | LOOM |
http://www.ebi.ac.uk/efo/EFO_0700036 | CCONT | LOOM |
http://www.ebi.ac.uk/efo/EFO_0700036 | EFO | LOOM |