Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.15 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes CHRNA3-related congenital anomalies of the kidney and urinary tract |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.195 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT, 191800 |
Component of the following Super Panels:
Signed-off version 5.10 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes CAKUT, dysautonomia, Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT, 191800 |