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BioAssay Ontology
Last uploaded:
February 21, 2024
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Preferred Name | Fabry disease | |
Synonyms |
alpha galactosidase deficiency Alpha-galactosidase A deficiency Fabry's disease Angiokeratoma Corporis Diffusum deficiency of melibiase |
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Definitions |
A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_14499 |
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comment |
OMIM mapping confirmed by DO. [SN].
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database_cross_reference |
ICD10CM:E75.21 SNOMEDCT_US_2020_03_01:16652001 UMLS_CUI:C0002986 MESH:D000795 OMIM:301500 GARD:6400 NCI:C84701
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has exact synonym |
alpha galactosidase deficiency Alpha-galactosidase A deficiency Fabry's disease Angiokeratoma Corporis Diffusum deficiency of melibiase
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has_obo_namespace |
disease_ontology
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id |
DOID:14499
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imported from | ||
in_subset | ||
label |
Fabry disease
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notation |
DOID:14499
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prefLabel |
Fabry disease
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textual definition |
A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22.
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subClassOf |
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