Panel | Mode of inheritance | Details |
---|---|---|
8 panels | ||
Green in CleftingComponent of the following Super Panels:
Signed-off version 5.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes ACROCALLOSAL SYNDROME, ACLS |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes ACROCALLOSAL SYNDROME 200990, AUTOSOMAL RECESSIVE MENTAL RETARDATION |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes AUTOSOMAL RECESSIVE MENTAL RETARDATION, ACROCALLOSAL SYNDROME |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 6.13 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Hydrolethalus syndrome 2, 614120Acrocallosal syndrome, 200990Joubert syndrome 12, 200990, ACROCALLOSAL SYNDROME |
Green in Neurological ciliopathiesComponent of the following Super Panels:
Signed-off version 4.1 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Joubert syndrome 12 200990, Acrocallosal syndrome 200990 |
Green in Ophthalmological ciliopathiesComponent of the following Super Panels:
Signed-off version 4.1 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Joubert syndrome 12 200990, Acrocallosal syndrome 200990 |
Green in Renal ciliopathiesComponent of the following Super Panels:
Signed-off version 3.7 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Joubert syndrome 12 200990, Acrocallosal syndrome 200990 |
Green in Skeletal dysplasiaComponent of the following Super Panels:
R-numbers: R104 Signed-off version 5.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Joubert syndrome 12 200990, Acrocallosal syndrome 200990, Al-Gazali-Bakalinova syndrome 607131, Hydrolethalus syndrome 2 614120 |