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| Structural eye disease v0.76 | FREM2 | Nicola Ragge reviewed gene: FREM2: Rating: GREEN; Mode of pathogenicity: ; Publications: 15838507; Phenotypes: FRASER SYNDROME 2, 617666; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | FREM2 | Ivone Leong reviewed gene: FREM2: Rating: GREEN; Mode of pathogenicity: ; Publications: 15838507; Phenotypes: FRASER SYNDROME 2 617666; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | FREM2 |
Ivone Leong Source NHS GMS was added to FREM2. Added phenotypes FRASER SYNDROME 2 617666 for gene: FREM2 Publications for gene FREM2 were changed from to 15838507 |
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| Structural eye disease v0.2 | FREM2 |
Ellen McDonagh gene: FREM2 was added gene: FREM2 was added to Structural eye disease. Sources: Expert Review Green Mode of inheritance for gene: FREM2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FREM2 were set to Eye Disorders |
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