Source: ANIMAL_MODELS

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: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0149940
Disease: Sciatic Neuropathy
Sciatic Neuropathy 		disease 0.200 None 1.000 2 0 1988 2002
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		disease 0.200 None 1.000 1 0 1996 1996
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		disease 0.200 None 1.000 1 0 2008 2008
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental 		disease 0.200 None 1.000 1 0 2003 2003
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		disease 0.200 None 1.000 1 0 1999 1999
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias 		group 0.200 None 1.000 1 0 1993 1993
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0043020
Disease: Wallerian Degeneration
Wallerian Degeneration 		phenotype 0.200 None 1.000 1 0 2000 2000
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal 		disease 0.200 None 1.000 1 0 1993 1993
Entrez Id: 4744
Gene Symbol: NEFH
NEFH 		neurofilament heavy 0.588 0.769 2.7E-12
CUI: C0342200
Disease: Endemic Cretinism
Endemic Cretinism 		disease 0.200 None 1.000 1 0 2008 2008