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: C1839326
Disease: Abnormal form of the vertebral bodies
Abnormal form of the vertebral bodies 		phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C1860243
Disease: Abnormal sternal ossification
Abnormal sternal ossification 		phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		phenotype 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: C4316903
Disease: Absence Seizures
Absence Seizures 		phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C1854882
Disease: Absent speech
Absent speech 		phenotype 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: C0001807
Disease: Aggressive behavior
Aggressive behavior 		phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		phenotype 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: 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: 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: C1271219
Disease: Congenital ectopic pupil
Congenital ectopic pupil 		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: C0265695
Disease: Congenital fusion of ribs
Congenital fusion of ribs 		disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		phenotype 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: 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: C1837108
Disease: Decreased muscle mass
Decreased muscle mass 		phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1 		complexin 1 0.576 0.654 0.82
CUI: C4023681
Disease: Delayed fine motor development
Delayed fine motor development 		phenotype 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