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"
481 to 490 of 495 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
Huntingtin
HD, IT15, LOMARS
Attention deficit hyperactivity disorder, Cerebral palsy, Major depressive disorder, Diffuse gastric adenocarcinoma, Dyslexia, Gastric cancer, Huntington disease, Metabolic syndrome, Mood disorder, Movement disorder, Myocardial infarction, Non-specific syndromic intellectual disability, Parkinson disease, Diabetes mellitus type 2

482
Hormonally up-regulated Neu-associated kinase
-
Astrocytoma, Crohn disease, Hearing loss, Inflammatory bowel disease, Periodontitis, Rosacea, Diabetes mellitus type 2, Vitiligo

483
HUS1 checkpoint clamp component B
-
Neurodevelopmental disorder

484
HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1
ARF-BP1, HECTH9, HSPC272, Ib772, LASU1, MRXST, MULE, URE-B1, UREB1
Atrial septal defect, Autism, Bipolar disorder, Global developmental delay, Hypothyroidism, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Intellectual developmental disorder hypotonic x-linked, Male infertility single gene azoospermia, Non-specific syndromic intellectual disability, X-linked intellectual disability, Say meyer syndrome, Diabetes mellitus type 2, Ventricular septal defect

485
Hydrogen voltage gated channel 1
HV1, VSOP
Atrial fibrillation, Gout

486
Hyaluronidase 1
HYAL-1, LUCA1, MPS9, NAT6
Hyaluronoglucosaminidase deficiency, Mucopolysaccharidosis, Schizophrenia

487
Hyaluronidase 2
LUCA2, MCCS
Alzheimer disease, Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome, Gastroesophageal reflux disease, Muggenthaler-chowdhury-chioza syndrome, Orofacial cleft, Peptic ulcer disease, Schizophrenia

488
Hyaluronidase 3
HYAL-3, LUCA-3, LUCA3
Auroneurodental syndrome, Metabolic syndrome, Diabetes mellitus type 2

489
Hyccin PI4KA lipid kinase complex subunit 1
DRCTNNB1A, FAM126A, HCC, HLD5
Astrocytoma, Bipolar disorder, Hypomyelinating leukodystrophy, Intellectual developmental disorder, Parkinson disease, Periodontitis, Scoliosis

490
Hyccin PI4KA lipid kinase complex subunit 2
FAM126B
Breast cancer, Lymphocytic leukemia, Non-melanoma skin carcinoma