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| Structural eye disease v0.76 | KLHL7 | Nicola Ragge reviewed gene: KLHL7: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 42, 612943; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | KLHL7 | Ivone Leong reviewed gene: KLHL7: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 42, 612943; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | KLHL7 |
Ivone Leong Source NHS GMS was added to KLHL7. Mode of inheritance for gene KLHL7 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Retinitis pigmentosa 42, 612943 for gene: KLHL7 |
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| Structural eye disease v0.2 | KLHL7 |
Ellen McDonagh gene: KLHL7 was added gene: KLHL7 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: KLHL7 was set to Phenotypes for gene: KLHL7 were set to Eye Disorders |
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