Panel | Mode of inheritance | Details |
---|---|---|
7 panels | ||
Green in CleftingComponent of the following Super Panels:
Signed-off version 6.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Culler-Jones syndrome, OMIM:615849, Holoprosencephaly 9, OMIM:610829 |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.6 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes GLI2-RELATED HOLOPROSENCEPHALY 261768 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes GLI2-RELATED HOLOPROSENCEPHALY |
Green in Holoprosencephaly - NOT chromosomalComponent of the following Super Panels:
R-numbers: R85 Signed-off version 5.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Holoprosencephaly-9, Holoprosencephaly, Holoprosencephaly 9, 610829 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 7.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Holoprosencephaly-9, 610829, GLI2-RELATED HOLOPROSENCEPHALY |
Green in Limb disordersComponent of the following Super Panels:
Signed-off version 6.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Holoprosencephaly 9 610829, Culler-Jones syndrome 615849, Polydactyly |
Green in Pituitary hormone deficiencyR-numbers: R159 Signed-off version 3.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Culler-Jones syndrome (615849), Holoprosencephaly 9 (610829) |