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| Structural eye disease v0.76 | TMEM138 | Nicola Ragge reviewed gene: TMEM138: Rating: RED; Mode of pathogenicity: ; Publications: 22282472; Phenotypes: Joubert syndrome 16, 614465; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | TMEM138 | Ivone Leong edited their review of gene: TMEM138: Changed phenotypes: Joubert syndrome 16, 614465 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | TMEM138 | Ivone Leong reviewed gene: TMEM138: Rating: RED; Mode of pathogenicity: ; Publications: 22282472; Phenotypes: Joubert syndrome 2, 608091, Meckel syndrome 2, 603194; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | TMEM138 |
Ivone Leong Source NHS GMS was added to TMEM138. Added phenotypes Joubert syndrome 16, 614465 for gene: TMEM138 |
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| Structural eye disease v0.2 | TMEM138 |
Ellen McDonagh gene: TMEM138 was added gene: TMEM138 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: TMEM138 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TMEM138 were set to 22282472 Phenotypes for gene: TMEM138 were set to Joubert syndrome |
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