Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q
0.900 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
0.220 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder)
0.200 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
Hereditary Motor and Sensory Neuropathies
0.200 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder)
0.200 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
0.200 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
Hereditary motor and sensory neuropathy, types I-IV
0.200 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
Peroneal muscular atrophy (axonal type) (hypertrophic type)
0.200 Biomarker MGD DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice. 29661920

2018

Entrez Id: 55526
Gene Symbol: DHTKD1
DHTKD1
Amino Acid Metabolism, Inborn Errors
0.200 Biomarker MGD