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Experimental Factor Ontology
Preferred Name | Fabry disease | |
Synonyms |
Fabry disease, Cardiac variant Gla deficiency ceramide trihexosidase deficiency angiokeratoma, diffuse hereditary dystopic lipidosis diffuse angiokeratoma angiokeratoma corporis diffusum Fabry's disease Alpha-galactosidase A deficiency alpha galactosidase deficiency Anderson-Fabry disease deficiency of melibiase Fabry disease FD Fd |
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Definitions |
Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0010526 |
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closeMatch | ||
curated_content_resource |
https://search.clinicalgenome.org/kb/conditions/MONDO:0010526 |
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database_cross_reference |
NANDO:2200563 MEDGEN:8083 NCIT:C84701 icd11.foundation:66996647 SCTID:16652001 UMLS:C0002986 MedDRA:10016016 Orphanet:324 MESH:D000795 NANDO:1200157 OMIM:301500 DOID:14499 GARD:6400 NORD:1115
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definition |
Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.
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exactMatch |
http://linkedlifedata.com/resource/umls/id/C0002986 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/66996647 http://identifiers.org/medgen/8083 http://identifiers.org/snomedct/16652001 http://identifiers.org/mesh/D000795 http://purl.obolibrary.org/obo/DOID_14499 |
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has_exact_synonym |
diffuse angiokeratoma angiokeratoma corporis diffusum Fabry's disease Alpha-galactosidase A deficiency alpha galactosidase deficiency Anderson-Fabry disease deficiency of melibiase Fabry disease FD Fd
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has_related_synonym |
Fabry disease, Cardiac variant Gla deficiency ceramide trihexosidase deficiency angiokeratoma, diffuse hereditary dystopic lipidosis
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IAO_0000233 | ||
id |
MONDO:0010526
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in_subset |
http://purl.obolibrary.org/obo/mondo#ordo_disorder http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare http://purl.obolibrary.org/obo/mondo#orphanet_rare http://purl.obolibrary.org/obo/mondo#otar |
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label |
Fabry disease
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notation |
MONDO:0010526
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preferred label |
Fabry disease
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prefLabel |
Fabry disease
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excluded_subClassOf |
http://purl.obolibrary.org/obo/MONDO_0016340 http://purl.obolibrary.org/obo/MONDO_0019293 http://purl.obolibrary.org/obo/MONDO_0019520 http://purl.obolibrary.org/obo/MONDO_0005328 |
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subClassOf |
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