Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes RENAL HYPODYSPLASIA/APLASIA 1 191830 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Renal hypodysplasia/aplasia 1, OMIM:191830, Renal hypodysplasia/aplasia 1, MONDO:0024519 |
Component of the following Super Panels:
Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes CAKUT, Renal hypodysplasia/aplasia 1, 191830 |
Component of the following Super Panels:
Signed-off version 1.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Renal hypodysplasia/aplasia 1, 191830 |