Disease: MYELOPROLIFERATIVE SYNDROME, TRANSIENT ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MYELOPROLIFERATIVE SYNDROME, TRANSIENT
CUI: C1834582
Disease: MYELOPROLIFERATIVE SYNDROME, TRANSIENT
0.010 GeneticVariation BEFREE A novel A-band titin mutation, c.92167C>T (p.P30723S), was found in 1 patient, and 1 Portuguese patient with a severe TMD phenotype proved to be homozygous for the previously reported Iberian TMD mutation. 24395473 2014