Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "H"
361 to 370 of 495 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
Hippocalcin
BDR2, DYT2
Movement disorder, Dystonia, Dystonia musculorum deformans, Genetic torsion dystonia, Torsion dystonia

362
Hippocalcin like 1
BDR1, HLP2, VILIP-3
Cataract, Cerebral amyloid angiopathy, Dental caries, Liver cirrhosis, Peripheral arterial disease, Hypertension

363
Hippocalcin like 4
HLP4
Attention deficit hyperactivity disorder, Glioma, Osteoarthritis, Substance abuse

364
4-hydroxyphenylpyruvate dioxygenase
4-HPPD, 4HPPD, GLOD3, HPPD, HPPDASE, PPD
Global developmental delay, Hypertyrosinemia, Obesity, Tyrosinemia

365
4-hydroxyphenylpyruvate dioxygenase like
4-HPPD-L, GLOXD1, NEDSWMA, SPG83
Spastic paraplegia, Leigh syndrome, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Spastic ataxia

366
15-hydroxyprostaglandin dehydrogenase
15-PGDH, PGDH, PGDH1, PHOAR1, SDR36C1
Biliary cirrhosis, Medullary carcinoma, Colorectal cancer, Cranioosteoarthropathy, Desbuquois syndrome, Digital clubbing, isolated congenital, Primary hypertrophic osteoarthropathy, Biliary cholangitis, Prostatic neoplasms, Thyroid neoplasms, Venous thromboembolism

367
Hematopoietic prostaglandin D synthase
GSTS, GSTS1, GSTS1-1, PGD2, PGDS
Bipolar disorder, Kidney neoplasms, Liver cirrhosis, Liver disease, Mood disorder, Psychotic disorders, Schizophrenia, Testicular carcinoma, Testicular germ cell tumor

368
Hepsin
TMPRSS1
Atrial fibrillation, Lipidoses, Lipoidosis, Intellectual developmental disorder, Prostatic neoplasms

369
Haptoglobin-related protein
A-259H10.2, HP
Cardiovascular disease, Coronary artery disease, Metabolic syndrome

370
Hypoxanthine phosphoribosyltransferase 1
HGPRT, HPRT
Gout, Hyperuricemia, Hyperuricemia syndrome, Neurotic disorder, Partial hypoxanthine-guanine phosphoribosyltransferase deficiency