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| Structural eye disease v0.76 | TTC21B | Nicola Ragge reviewed gene: TTC21B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY, 613819; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | TTC21B | Ivone Leong edited their review of gene: TTC21B: Changed phenotypes: SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY, 613819 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | TTC21B | Ivone Leong reviewed gene: TTC21B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 51, 613464, Bardet-Biedl syndrome 8, 615985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | TTC21B |
Ivone Leong Source NHS GMS was added to TTC21B. Mode of inheritance for gene TTC21B was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY, 613819 for gene: TTC21B |
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| Structural eye disease v0.2 | TTC21B |
Ellen McDonagh gene: TTC21B was added gene: TTC21B was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: TTC21B was set to Phenotypes for gene: TTC21B were set to Eye Disorders |
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