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: C0036572
Disease: Seizures
Seizures
phenotype 0.110 None 1.000 0 0 2014 2014
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group 0.110 None 1.000 0 0 2017 2017
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C1840380
Disease: Persistent cavum septum pellucidum
Persistent cavum septum pellucidum
phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C1844825
Disease: Hyperconvex fingernails
Hyperconvex fingernails
phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
Photosensitive tonic-clonic seizures
disease 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C1848977
Disease: Short upper lip
Short upper lip
phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C1853237
Disease: Isolated cases
Isolated cases
phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C1853242
Disease: Midface retrusion
Midface retrusion
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: C1855728
Disease: Low posterior hairline
Low posterior hairline
phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
CUI: C1839858
Disease: Periventricular cysts
Periventricular cysts
phenotype 0.100 None 0 0
Entrez Id: 10815
Gene Symbol: CPLX1
CPLX1
complexin 1 0.576 0.654 0.82
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: 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: 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: 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: C0848558
Disease: Hypospadias
Hypospadias
disease 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: 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: 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
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: 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: 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: C1836830
Disease: Developmental regression
Developmental regression
disease 0.100 None 0 0