Source: MGD

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C3151136
Disease: CILIARY DYSKINESIA, PRIMARY, 14
CILIARY DYSKINESIA, PRIMARY, 14 		disease 0.900 None 1.000 0 0 2011 2014
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		disease 0.310 None 1.000 2 0 2011 2018
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		disease 0.230 None 1.000 0 0 2012 2014
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C0478019
Disease: Other specified congenital malformations of respiratory system
Other specified congenital malformations of respiratory system 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		disease 0.200 None 0 0
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39 		coiled-coil domain containing 39 0.641 0.615 7.9E-12
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		disease 0.200 None 0 0