Source: CLINVAR

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: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.400 strong 1.000 0 1 2013 2013
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0036572
Disease: Seizures
Seizures 		phenotype 0.400 strong 1.000 0 1 2013 2013
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C4072903
Disease: Primary Caesarian section
Primary Caesarian section 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0238210
Disease: Malrotation of kidney
Malrotation of kidney 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0576227
Disease: Narrow foot
Narrow foot 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0578038
Disease: Thin lips
Thin lips 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C3693299
Disease: Broad uvula
Broad uvula 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C1845447
Disease: Cupped ears (finding)
Cupped ears (finding) 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C1843367
Disease: Poor school performance
Poor school performance 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C1835762
Disease: Widely-spaced maxillary central incisors
Widely-spaced maxillary central incisors 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C1305740
Disease: Overbite
Overbite 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C1142533
Disease: Smooth philtrum
Smooth philtrum 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval 		phenotype 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0018536
Disease: Hallux Valgus
Hallux Valgus 		disease 0.100 None 0 1
Entrez Id: 81603
Gene Symbol: TRIM8
TRIM8 		tripartite motif containing 8 0.588 0.731 0.99
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		disease 0.100 None 0 1