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| Structural eye disease v0.76 | INVS | Nicola Ragge reviewed gene: INVS: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Nephronophthisis 2, infantile, 602088; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | INVS | Ivone Leong reviewed gene: INVS: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Nephronophthisis 2, infantile, 602088; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | INVS |
Ivone Leong Source NHS GMS was added to INVS. Mode of inheritance for gene INVS was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Nephronophthisis 2, infantile, 602088 for gene: INVS |
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| Structural eye disease v0.2 | INVS |
Ellen McDonagh gene: INVS was added gene: INVS was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: INVS was set to Phenotypes for gene: INVS were set to Eye Disorders |
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