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The Biomarker Ontology
Last uploaded:
June 3, 2024
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Preferred Name | Fabry disease | |
Synonyms |
Fabry Disease, Cardiac Variant 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 UMLS_CUI:C0002986 MESH:D000795 SNOMEDCT_US_2022_09_01:16652001 OMIM:301500 GARD:6400 NCI:C84701
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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. OMIM mapping confirmed by DO. [SN].
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fromOldVersion |
yes
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has_obo_namespace |
disease_ontology
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hasExactSynonym |
Fabry Disease, Cardiac Variant alpha galactosidase deficiency Alpha-galactosidase A deficiency Fabry's disease Angiokeratoma Corporis Diffusum deficiency of melibiase
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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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note |
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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preferred label |
Fabry disease
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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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