Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 144568
Gene Symbol: A2ML1
A2ML1
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.600 GermlineCausalMutation ORPHANET Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. 24939586

2015