Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes INTELLECTUAL DISABILITY |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Neurodevelopmental disorder with hypotonia, impaired language, and dysmorphic features, OMIM:616579 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 6.13 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Neurodevelopmental disorder with hypotonia, impaired language, and dysmorphic features, OMIM:616579 |
Green in Severe microcephalyR-numbers: R88 Signed-off version 5.7 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Mental retardation, autosomal dominant 40, OMIM:616579 |