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Structural eye disease v0.76 | MTTP | Nicola Ragge reviewed gene: MTTP: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Abetalipoproteinemia, 200100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.48 | MTTP | Ivone Leong edited their review of gene: MTTP: Changed phenotypes: Abetalipoproteinemia, 200100 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.38 | MTTP | Ivone Leong reviewed gene: MTTP: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 1B, 276900, Deafness, autosomal recessive 2, Deafness, autosomal dominant 11, 601317 ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.15 | MTTP |
Ivone Leong Source NHS GMS was added to MTTP. Mode of inheritance for gene MTTP was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Abetalipoproteinemia, 200100 for gene: MTTP |
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Structural eye disease v0.2 | MTTP |
Ellen McDonagh gene: MTTP was added gene: MTTP was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: MTTP was set to Phenotypes for gene: MTTP were set to Eye Disorders |