Disease: MUNGAN SYNDROME ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MUNGAN SYNDROME
CUI: C1969653
Disease: MUNGAN SYNDROME
0.800 CausalMutation CLINVAR Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstruction. 25575569 2015
MUNGAN SYNDROME
CUI: C1969653
Disease: MUNGAN SYNDROME
0.800 GeneticVariation UNIPROT