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| Structural eye disease v0.76 | FREM1 | Nicola Ragge reviewed gene: FREM1: Rating: GREEN; Mode of pathogenicity: ; Publications: 21507892, ; Phenotypes: MANITOBA OCULOTRICHOANAL SYNDROME, 248450; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | FREM1 | Ivone Leong reviewed gene: FREM1: Rating: GREEN; Mode of pathogenicity: ; Publications: 21507892; Phenotypes: MANITOBA OCULOTRICHOANAL SYNDROME 248450; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | FREM1 |
Ivone Leong Source NHS GMS was added to FREM1. Added phenotypes MANITOBA OCULOTRICHOANAL SYNDROME 248450 for gene: FREM1 Publications for gene FREM1 were changed from to 21507892 |
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| Structural eye disease v0.2 | FREM1 |
Ellen McDonagh gene: FREM1 was added gene: FREM1 was added to Structural eye disease. Sources: Expert Review Green Mode of inheritance for gene: FREM1 was set to BIALLELIC, autosomal or pseudoautosomal |
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