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| Structural eye disease v0.76 | CLN5 | Nicola Ragge reviewed gene: CLN5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 5, 256731; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CLN5 | Ivone Leong reviewed gene: CLN5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 5, 256731; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CLN5 |
Ivone Leong Source NHS GMS was added to CLN5. Mode of inheritance for gene CLN5 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Ceroid lipofuscinosis, neuronal, 5, 256731 for gene: CLN5 |
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| Structural eye disease v0.2 | CLN5 |
Ellen McDonagh gene: CLN5 was added gene: CLN5 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CLN5 was set to Phenotypes for gene: CLN5 were set to Eye Disorders |
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