Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
6001 to 6010 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6001
Hydroxysteroid 11-beta dehydrogenase 2
AME, AME1, HSD11K, HSD2, SDR9C3
Mineralocortocoid excess, Asthma, Diabetes mellitus type 1, Hypertension, Liver cirrhosis, Myocardial infarction, Nephrotic syndrome, Obesity

6002
Hydroxysteroid 17-beta dehydrogenase 1
17-beta-HSD, 20-alpha-HSD, E2DH, EDH17B2, EDHB17, HSD17, SDR28C1
Autism, Endometriosis, Metabolic syndrome, Prostatic neoplasms, Diabetes mellitus type 2

6003
Hydroxysteroid 17-beta dehydrogenase 10
17b-HSD10, ABAD, CAMR, DUPXp11.22, ERAB, HADH2, HCD2, HSD10MD, MHBD, MRPP2, MRX17, MRX31, MRXS10, SCHAD, SDR5C1
Chorea, Intellectual developmental disorder, x-linked

6004
Hydroxysteroid 17-beta dehydrogenase 11
17-BETA-HSD11, 17-BETA-HSDXI, 17BHSD11, DHRS8, PAN1B, RETSDR2, SDR16C2
Gout, Major depressive disorder

6005
Hydroxysteroid 17-beta dehydrogenase 12
KAR, SDR12C1
Astrocytoma, Attention deficit hyperactivity disorder, Cardiovascular disease, Coronary artery disease, Melanoma, Hypertension, Hyperopia, Metabolic syndrome, Neuroblastoma, Scoliosis, Substance abuse, Diabetes mellitus type 2

6006
Hydroxysteroid 17-beta dehydrogenase 13
FLDP, HMFN0376, NIIL497, SCDR9, SDR16C3
Liver cirrhosis, Nonalcoholic fatty liver disease

6007
Hydroxysteroid 17-beta dehydrogenase 14
DHRS10, SDR47C1, retSDR3
Myopia

6008
Hydroxysteroid 17-beta dehydrogenase 2
EDH17B2, HSD17, SDR9C2
Breast cancer, Endometrial neoplasms, Endometriosis

6009
Hydroxysteroid 17-beta dehydrogenase 3
EDH17B3, SDR12C2
17-beta-hydroxysteroid dehydrogenase deficiency, 46,xy disorder of sex developmen, Disorders of sex development, Myoclonic epilepsy, Prostatic neoplasms

6010
Hydroxysteroid 17-beta dehydrogenase 4
DBP, MFE-2, MFP-2, MPF-2, PRLTS1, SDR8C1
Bifunctional enzyme deficiency, Congenital neurologic anomalies, Cryptogenic west syndrome, D-bifunctional protein deficiency, Fatty acid metabolism disorder, Essential tremor, Gonadal dysgenesis, Major depressive disorder, Peroxisomal disorder, Perrault syndrome, Infantile spasms, West syndrome, Xx gonadal dysgenesis syndrome