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| Structural eye disease v0.76 | MKKS | Nicola Ragge reviewed gene: MKKS: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome 6, McKusick-Kaufman syndrome, 605231, 236700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | MKKS | Ivone Leong edited their review of gene: MKKS: Changed phenotypes: Bardet-Biedl syndrome 6, McKusick-Kaufman syndrome, 605231, 236700 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | MKKS | Ivone Leong reviewed gene: MKKS: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Bardet-Biedl syndrome 13, 615990, Meckel syndrome 1, 249000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | MKKS |
Ivone Leong Source NHS GMS was added to MKKS. Mode of inheritance for gene MKKS was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Bardet-Biedl syndrome 6; 605231; McKusick-Kaufman syndrome; 236700 for gene: MKKS |
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| Structural eye disease v0.2 | MKKS |
Ellen McDonagh gene: MKKS was added gene: MKKS was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: MKKS was set to Phenotypes for gene: MKKS were set to Eye Disorders |
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