Source: ALL

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: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		disease 0.800 strong 1.000 11 8 2009 2019
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C2750747
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C 		disease 0.600 None 1.000 5 19 2009 2016
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		disease 0.310 None 1.000 1 0 2012 2012
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C1848172
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A 		disease 0.300 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		group 0.300 limited 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C1850362
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B 		disease 0.300 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C3495587
Disease: Night Blindness, Congenital Stationary, Type 1A
Night Blindness, Congenital Stationary, Type 1A 		disease 0.300 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		disease 0.300 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C3501847
Disease: Night blindness, congenital stationary, type 1
Night blindness, congenital stationary, type 1 		disease 0.300 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb 		disease 0.300 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		disease 0.300 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		disease 0.110 None 0.500 2 1 2011 2018
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0028738
Disease: Nystagmus
Nystagmus 		disease 0.110 None 1.000 1 0 2018 2018
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		disease 0.110 None 1.000 1 0 2018 2018
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		disease 0.110 None 1.000 1 1 2017 2017
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0038379
Disease: Strabismus
Strabismus 		disease 0.110 None 1.000 1 0 2018 2018
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0025202
Disease: melanoma
melanoma 		disease 0.100 None 0.923 13 0 2004 2020
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		phenotype 0.100 None 1.000 1 1 2012 2012
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		disease 0.100 None 1.000 1 1 2016 2016
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0027092
Disease: Myopia
Myopia 		disease 0.100 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0271183
Disease: Severe myopia
Severe myopia 		disease 0.100 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		phenotype 0.100 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		disease 0.100 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C0151908
Disease: Dry skin
Dry skin 		phenotype 0.100 None 0 0
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		transient receptor potential cation channel subfamily M member 1 0.626 0.462 1.6E-42
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0