Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 5.48 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes MILROY DISEASE 153100 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 5.80 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes MILROY DISEASE |
Green in Primary lymphoedemaR-numbers: R136 Signed-off version 3.13 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Lymphedema, hereditary, IA 153100 |
Green in Vascular skin disordersR-numbers: R326 Signed-off version 1.65 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Hemangioma, capillary infantile, somatic, OMIM:602089 |