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| Structural eye disease v0.76 | CHMP4B | Nicola Ragge reviewed gene: CHMP4B: Rating: RED; Mode of pathogenicity: ; Publications: 17701905; Phenotypes: Cataract 31, multiple types, 605387; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.49 | CHMP4B | Ivone Leong edited their review of gene: CHMP4B: Changed phenotypes: Cataract 31, multiple types, 605387 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.39 | CHMP4B | Ivone Leong reviewed gene: CHMP4B: Rating: RED; Mode of pathogenicity: ; Publications: 17701905; Phenotypes: Megalocornea 1, X-linked, 309300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.13 | CHMP4B |
Ivone Leong gene: CHMP4B was added gene: CHMP4B was added to Structural eye disease. Sources: NHS GMS Mode of inheritance for gene: CHMP4B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CHMP4B were set to 17701905 Phenotypes for gene: CHMP4B were set to Cataract 31, multiple types, 605387 |
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