Panel | Mode of inheritance | Details |
---|---|---|
5 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 3.79 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes INSULIN-LIKE GROWTH FACTOR I DEFICIENCY 608747 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 3.122 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes INSULIN-LIKE GROWTH FACTOR I DEFICIENCY |
Green in Growth failure in early childhoodR-numbers: R147 Signed-off version 3.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Insulin-Like Growth Factor I Deficiency, Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747, IGF1 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 5.343 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747, INSULIN-LIKE GROWTH FACTOR I DEFICIENCY (IGF1 DEFICIENCY) |
Green in Severe microcephalyR-numbers: R88 Signed-off version 4.41 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Growth retardation with deafness and mental retardation due to IGF1 deficiency, 608747, MPD, microcephalic primordial dwarfism |