HMX3, H6 family homeobox 3, 340784

N. diseases: 4; N. variants: 0
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Otorhinolaryngologic Diseases Congenital Abnormality 137 5 0.010 None 1.000 1 2009 2009
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 68 17 0.010 None 1.000 1 2009 2009
CUI: C3275929
Disease: Superior semicircular canal dehiscence syndrome
Superior semicircular canal dehiscence syndrome 		disease Otorhinolaryngologic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2012 2012
CUI: C4523999
Disease: Superior semicircular canal dehiscence
Superior semicircular canal dehiscence 		disease Disease or Syndrome 1 0.010 None 1.000 1 2012 2012