MYH9-related disorder
blood platelet disease that has material basis in mutations in the MYH9 gene. It is characterized by thrombocytopenia, enlarged platelets, sensorineural hearing loss and presenile cataract
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MYH9-related disorder
Summary
MYH9-related disorder is a class of disease[1].
Key Facts
- MYH9-related disorder's instance of is recorded as class of disease[2].
- MYH9-related disorder's subclass of is recorded as blood platelet disease[3].
- MYH9-related disorder's subclass of is recorded as Inherited giant platelet disorder[4].
- MYH9-related disorder's OMIM ID is recorded as 155100[5].
- MYH9-related disorder's KEGG ID is recorded as H00233[6].
- MYH9-related disorder's Disease Ontology ID is recorded as DOID:0060651[7].
- MYH9-related disorder's Orphanet ID is recorded as 182050[8].
- MYH9-related disorder's genetic association is recorded as MYH9[9].
- MYH9-related disorder's Google Knowledge Graph ID is recorded as /g/15dpxjbn[10].
- MYH9-related disorder's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060651[11].
- MYH9-related disorder's exact match is recorded as http://identifiers.org/doid/DOID:0060651[12].
- MYH9-related disorder's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_182050[13].
- MYH9-related disorder's UMLS CUI is recorded as C5200934[14].
- MYH9-related disorder's ICD-10-CM is recorded as D69.4[15].
- MYH9-related disorder's GARD rare disease ID is recorded as 180[16].
- MYH9-related disorder's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- MYH9-related disorder's Genetics Home Reference Conditions ID is recorded as myh9-related-disorder[18].
- MYH9-related disorder's ICD-11 ID is recorded as 109013938[19].
- MYH9-related disorder's Experimental Factor Ontology ID is recorded as 0009646[20].