Preferred Name | Leber Congenital Amaurosis | |
Synonyms |
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Definitions |
A congenital retinopathy that is associated with mutation(s) in at least eighteen genes, typically characterized by severe visual impairment. |
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ID |
http://purl.obolibrary.org/obo/NCIT_C129075 |
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code |
C129075 |
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Contributing_Source |
Cellosaurus |
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definition |
A congenital retinopathy that is associated with mutation(s) in at least eighteen genes, typically characterized by severe visual impairment. |
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in_subset | ||
label |
Leber Congenital Amaurosis |
|
Preferred_Name |
Leber Congenital Amaurosis |
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prefixIRI |
NCIT:C129075 |
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prefLabel |
Leber Congenital Amaurosis |
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Semantic_Type |
Disease or Syndrome |
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UMLS_CUI |
C3553847 |
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subClassOf |
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