loading...| Preferred Name | MYH-9 related disease | |
| Synonyms |
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| Definitions |
A 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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| ID |
http://purl.obolibrary.org/obo/DOID_0060651 |
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| database_cross_reference |
OMIM:155100 ORDO:182050 ICD10CM:D69.4 |
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| definition |
A 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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| has_obo_namespace |
disease_ontology |
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| IAO_0000115 |
A 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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| id |
DOID:0060651 |
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| label |
MYH-9 related disease |
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| notation |
DOID:0060651 |
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| note |
A 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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| prefLabel |
MYH-9 related disease |
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| subClassOf |