Source: INFERRED

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: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C3554399
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F 		disease 0.800 None 1.000 0 4 2013 2017
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		disease 0.720 strong 1.000 0 0 2013 2019
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		disease 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		disease 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C0027092
Disease: Myopia
Myopia 		disease 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C0271183
Disease: Severe myopia
Severe myopia 		disease 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		phenotype 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C0038379
Disease: Strabismus
Strabismus 		disease 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C0028738
Disease: Nystagmus
Nystagmus 		disease 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		disease 0.100 None 0 0
Entrez Id: 345193
Gene Symbol: LRIT3
LRIT3 		leucine rich repeat, Ig-like and transmembrane domains 3 0.716 0.115 2.0E-11
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0