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: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0013362
Disease: Dysarthria
Dysarthria 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1834696
Disease: Hyporeflexia of lower limbs
Hyporeflexia of lower limbs 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1836012
Disease: Hyperreflexia proximally
Hyperreflexia proximally 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1836451
Disease: Distal lower limb amyotrophy
Distal lower limb amyotrophy 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1842587
Disease: Sensory axonal neuropathy
Sensory axonal neuropathy 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1848736
Disease: Distal amyotrophy
Distal amyotrophy 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1849134
Disease: Impaired vibration sensation in the lower limbs
Impaired vibration sensation in the lower limbs 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1854301
Disease: Motor delay
Motor delay 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1858285
Disease: Decreased number of peripheral myelinated nerve fibers
Decreased number of peripheral myelinated nerve fibers 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C2749625
Disease: Motor axonal neuropathy
Motor axonal neuropathy 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0020458
Disease: Hyperhidrosis disorder
Hyperhidrosis disorder 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0022821
Disease: Kyphosis deformity of spine
Kyphosis deformity of spine 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0028738
Disease: Nystagmus
Nystagmus 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		disease 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		phenotype 0.100 None 0 0
Entrez Id: 64837
Gene Symbol: KLC2
KLC2 		kinesin light chain 2 0.736 0.346 0.98
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		disease 0.100 None 0 0