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| Term | hereditary night blindness | ID (Ontology) | DOID:8498 (Human Disease) |
| Definition | |||
| Also Known As | "Congenital night blindness" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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retinal disease |__night blindness |__hereditary night blindness 23 rec. |__congenital stationary night blindness 23 rec. |__congenital stationary night blindness 1A 2 rec. |__congenital stationary night blindness 1B 4 rec. |__congenital stationary night blindness 1C 1 rec. |__congenital stationary night blindness 1D 1 rec. |__congenital stationary night blindness 1E 3 rec. |__congenital stationary night blindness 1F 1 rec. |__congenital stationary night blindness 1G 1 rec. |__congenital stationary night blindness 1H 2 rec. |__congenital stationary night blindness 2A 1 rec. |__congenital stationary night blindness autosomal dominant 1 |__congenital stationary night blindness autosomal dominant 2 1 rec. |__congenital stationary night blindness autosomal dominant 3 1 rec. |__Oguchi disease-1 4 rec. |__Oguchi disease-2 1 rec. |
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Relationships
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| Is a | night blindness | ||
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External Crossreferences & Linkouts
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ICD10CM:H53.63 ICD9CM:368.61 MESH:C537743 SNOMEDCT_US_2023_03_01:193687000 UMLS_CUI:C1306122 |
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