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| Structural eye disease v0.76 | CLN3 | Nicola Ragge reviewed gene: CLN3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 3, 204200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CLN3 | Ivone Leong reviewed gene: CLN3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 3, 204200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CLN3 |
Ivone Leong Source NHS GMS was added to CLN3. Mode of inheritance for gene CLN3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Ceroid lipofuscinosis, neuronal, 3, 204200 for gene: CLN3 |
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| Structural eye disease v0.2 | CLN3 |
Ellen McDonagh gene: CLN3 was added gene: CLN3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CLN3 was set to Phenotypes for gene: CLN3 were set to Eye Disorders |
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