Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Differences in sex developmentR-numbers: R146 Signed-off version 4.5 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Genital Anomalies and Suspected Adrenal Problems Gene Panel (UKGTN), Endocrine disorders including disorders of sexual development (Emory), congenital adrenal hyperplasia, 17,20-lyase deficiency, isolated 202110 and 17-alpha-hydroxylase/17,20-lyase deficiency 202110 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 17-alpha-hydroxylase/17,20-lyase deficiency, 17,20-lyase deficiency, isolated |