| Panel | Mode of inheritance | Details |
|---|---|---|
6 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.15 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes SYNDROMIC INTELLECTUAL DISABILITY 612100 |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 6.9 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Global developmental delay, Intellectual disability, Seizures, Abnormality of the eye, Abnormality of nervous system morphology, Hearing abnormality, Abnormality of the cardiovascular system, Abnormality of the skeletal system, Abnormality of the genitourinary system, Neurooculocardiogenitourinary syndrome, OMIM:618652 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.195 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Neurooculocardiogenitourinary syndrome, OMIM:618652 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 7.51 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Global developmental delay, Intellectual disability, Seizures, Abnormality of the eye, Abnormality of nervous system morphology, Hearing abnormality, Abnormality of the cardiovascular system, Abnormality of the skeletal system, Abnormality of the genitourinary system, Neurooculocardiogenitourinary syndrome, OMIM:618652 |
Green in Severe microcephalyR-numbers: R88 Signed-off version 6.8 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Neurooculocardiogenitourinary syndrome, OMIM:618652 |
Green in Structural eye diseaseR-numbers: R36 Signed-off version 4.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes corneal opacity, Peters anomaly, coloboma, microcornea, Neurooculocardiogenitourinary syndrome, OMIM:61865, MONDO:0032850 |