Source: HPO

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: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0018916
Disease: Hemangioma
Hemangioma 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C3495489
Disease: Rieger eye malformation sequence
Rieger eye malformation sequence 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C4025320
Disease: Craniofacial asymmetry
Craniofacial asymmetry 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0025990
Disease: Micrognathism
Micrognathism 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0033377
Disease: Ptosis
Ptosis 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0917796
Disease: Optic Atrophy, Hereditary, Leber
Optic Atrophy, Hereditary, Leber 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0013336
Disease: Dwarfism
Dwarfism 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0034013
Disease: Precocious Puberty
Precocious Puberty 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0265341
Disease: Rieger syndrome
Rieger syndrome 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0431371
Disease: Absence of septum pellucidum
Absence of septum pellucidum 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0920299
Disease: Overriding toe
Overriding toe 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C1836830
Disease: Developmental regression
Developmental regression 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0013362
Disease: Dysarthria
Dysarthria 		disease 0.100 None 0 0