TYMP, thymidine phosphorylase, 1890

N. diseases: 246; N. variants: 74
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030554
Disease: Paresthesia
Paresthesia 		0.100 Biomarker phenotype HPO
CUI: C0042963
Disease: Vomiting
Vomiting 		0.100 Biomarker phenotype HPO
CUI: C0152020
Disease: Gastroparesis
Gastroparesis 		0.100 Biomarker disease HPO
CUI: C0162292
Disease: External Ophthalmoplegia
External Ophthalmoplegia 		0.100 Biomarker disease HPO
CUI: C0162429
Disease: Malnutrition
Malnutrition 		0.100 Biomarker disease HPO
CUI: C0232462
Disease: Decrease in appetite
Decrease in appetite 		0.100 Biomarker phenotype HPO
CUI: C0234146
Disease: Absent reflex
Absent reflex 		0.100 Biomarker phenotype HPO
CUI: C0239181
Disease: Intermittent diarrhea
Intermittent diarrhea 		0.100 Biomarker phenotype HPO
CUI: C0262918
Disease: Extraocular Muscle Paresis
Extraocular Muscle Paresis 		0.100 CausalMutation disease CLINVAR
CUI: C0268630
Disease: Hyper-beta-alaninemia
Hyper-beta-alaninemia 		0.100 Biomarker phenotype HPO
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy 		0.100 Biomarker disease HPO
CUI: C0345200
Disease: Congenital dysmotility of small intestine
Congenital dysmotility of small intestine 		0.100 Biomarker disease HPO
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		0.100 Biomarker phenotype HPO
CUI: C0497327
Disease: Dementia
Dementia 		0.100 Biomarker disease HPO
CUI: C0948163
Disease: Leukoaraiosis
Leukoaraiosis 		0.100 Biomarker phenotype HPO
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism 		0.100 Biomarker disease HPO
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		0.100 Biomarker disease HPO
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		0.100 Biomarker disease HPO
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		0.100 Biomarker disease HPO
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		0.100 Biomarker phenotype HPO
CUI: C1836923
Disease: Gastrointestinal dysmotility
Gastrointestinal dysmotility 		0.100 CausalMutation phenotype CLINVAR
CUI: C1836923
Disease: Gastrointestinal dysmotility
Gastrointestinal dysmotility 		0.100 Biomarker phenotype HPO
CUI: C1837098
Disease: Easy fatigability
Easy fatigability 		0.100 Biomarker phenotype HPO
CUI: C1837108
Disease: Decreased muscle mass
Decreased muscle mass 		0.100 Biomarker phenotype HPO
CUI: C1837256
Disease: Macrovesicular hepatic steatosis
Macrovesicular hepatic steatosis 		0.100 Biomarker phenotype HPO