Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.6 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MICROPHTHALMIA SYNDROMIC TYPE 9 601186 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes MICROPHTHALMIA SYNDROMIC TYPE 9 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Microphthalmia, syndromic 9, 601186Microphthalmia, isolated, with coloboma 8, 601186, MICROPHTHALMIA SYNDROMIC TYPE 9 (MCOPS9) |
Green in Structural eye diseaseR-numbers: R36 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Microphthalmia, syndromic 9, 601186, Microphthalmia, isolated, with coloboma 8, 601186, Syndromic Microphthalmia, Recessive |