SPRED2

sprouty related EVH1 domain containing 2
OMIM: 609292, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green SPRED2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Noonan syndrome 14, MIM# 619745
Green SPRED2 in Mendeliome Version 1.2302	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Noonan syndrome 14, MIM# 619745
Green SPRED2 in Rasopathy Level 2: Dysmorphic and congenital abnormality syndromes Version 0.105	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Noonan syndrome 14, MIM# 619745
Green SPRED2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Noonan syndrome 14, MIM# 619745
Amber SPRED2 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.196	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Noonan syndrome 14, MIM# 619745
Green SPRED2 in Growth failure Version 1.76	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Noonan syndrome 14, MIM# 619745
Green SPRED2 in Fetal anomalies Version 1.313	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Expert list Phenotypes Noonan syndrome 14, MIM# 619745