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Health_ontology
Last uploaded:
July 4, 2024
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Preferred Name | cystinosis | |
Synonyms |
cystine storage disease |
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Definitions |
A lysosomal storage disease characterized by the abnormal accumulation of cystine in the lysosomes. It follows an autosomal recessive inheritance pattern and that has_material_basis_in mutations in the CTNS gene, located on chromosome 17. |
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ID |
http://purl.obolibrary.org/obo/DOID_1064 |
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alternative label |
cystine storage disease
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database_cross_reference |
SNOMEDCT_US_2023_03_01:62332007 NCI:C129932 UMLS_CUI:C2931187 MESH:D003554 GARD:6236 MIM:219750 MIM:219800 MIM:219900 ORDO:213
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definition |
A lysosomal storage disease characterized by the abnormal accumulation of cystine in the lysosomes. It follows an autosomal recessive inheritance pattern and that has_material_basis_in mutations in the CTNS gene, located on chromosome 17.
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has exact synonym |
cystine storage disease
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has material basis in | ||
has_obo_namespace |
disease_ontology
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id |
DOID:1064
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in_subset | ||
label |
cystinosis
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notation |
DOID:1064
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prefLabel |
cystinosis
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subClassOf |
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