RPS23

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber RPS23 in Hypertrichosis syndromes Level 2: Dysmorphic and congenital abnormality syndromes Version 0.46	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Brachycephaly, trichomegaly, and developmental delay, MIM# 617412
Amber RPS23 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Brachycephaly, trichomegaly, and developmental delay, MIM# 617412
Amber RPS23 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Genetic Health Queensland Phenotypes Brachycephaly, trichomegaly, and developmental delay, MIM# 617412
Amber RPS23 in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Genomics England PanelApp Genetic Health Queensland Phenotypes Brachycephaly, trichomegaly, and developmental delay, MIM# 617412

4 panels