201
|
|
|
2-hydroxyacyl-CoA lyase 1 |
2-HPCL, HPCL, HPCL2, PHYH2 |
Curated: Alzheimer disease, Cholelithiasis
Unreviewed: N/A
|
202
|
|
|
2-hydroxyacyl-CoA lyase 2 |
209L8, AHAS, HACL1L, ILV2H, ILVBL |
Curated: N/A
Unreviewed: Asthma, Respiratory system infectious disease
|
203
|
|
|
Hydroxyacyl-CoA dehydrogenase |
HAD, HADH1, HADHSC, HCDH, HHF4, MSCHAD, SCHAD |
Curated: 3-hydroxyacyl-coa dehydrogenase deficiency, Congenital hyperinsulinism, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Obesity, Amyotrophic lateral sclerosis, obsolete hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Unreviewed: 3-hydroxyacyl-CoA Dehydrogenase Deficiency, Adrenoleukodystrophy, Cardiomyopathy, Colorectal neoplasm, Congestive Heart Failure, Diabetes Mellitus, Fatty Liver, Heart Failure, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoglycemic coma, Hypoglycemic encephalopathy, Hypoglycemic seizures, Hypotonia, Laryngeal carcinoma, Laryngeal neoplasm, Larynx cancer, Liver failure, Liver neoplasm, Malignant Neoplasm, Mental retardation, Metabolic Diseases, Metabolic Syndrome, Mitochondrial disease, Mitochondrial trifunctional protein deficiency, Motor delay, Nervous System Diseases, Non-Alcoholic Fatty Liver Disease, Renal cell carcinoma, Retinitis Pigmentosa, Squamous cell carcinoma, Stomach neoplasms
|
204
|
|
|
Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha |
ECHA, GBP, HADH, LCEH, LCHAD, MLCL AT, MTPA, TP-ALPHA |
Curated: Alzheimer disease, Fatty liver, Fatty liver, alcoholic, Myocardial ischemia, Osteoarthritis, Trifunctional protein deficiency, long chain 3-hydroxyacyl-coa dehydrogenase deficiency
Unreviewed: Abetalipoproteinemia, Adrenogenital Syndrome, Alpha 1-Antitrypsin Deficiency, Amyotrophic Lateral Sclerosis, Arthritis, Breast Cancer, Cardiomyopathy, Cardiovascular disease, Carnitine palmitoyl transferase deficiency, Carnitine-Acylcarnitine Translocase Deficiency, Cholestasis, Cholestatic liver disease, Chondrodysplasia, Chorioretinal atrophy, Congenital abnormalities, Congenital adrenal hyperplasia, Congenital Clubfoot, Congestive Heart Failure, Cytochrome-C Oxidase Deficiency, Developmental Delay, Diabetes Mellitus, Disorder Of Skeletal Muscle, Distal peripheral sensory neuropathy, Dyslipidemias, Exotropia, Fatty Liver, Glycogen Storage Disease, Heart Failure, HELLP Syndrome, Hepatocellular carcinoma, Hydrops Fetalis, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoparathyroidism, Inborn Errors Of Metabolism, Inflammatory Bowel Disease, Ischemic Stroke, Left Ventricular Hypertrophy, Liver disease, Liver failure, Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Lung Cancer, Lung carcinoma, Lung Neoplasms, Lymphohistiocytosis, Lymphoma, Mental retardation, Metabolic Diseases, Metabolic syndrome, Mitochondrial trifunctional protein deficiency, Motor delay, Multiple Congenital Anomalies, Myocardial Ischemia, Myopathy, Myopia, Neoplasms, Nervous System Diseases, Nyctalopia, Obesity, Osteoarthrosis Deformans, Pancreatic neoplasm, Peripheral Neuropathy, Prostate cancer, Prostatitis, Renal cell carcinoma, Respiratory Distress Syndrome, Respiratory Failure, Retinal Diseases, Retinitis Pigmentosa, Rhabdomyolysis, Sensorimotor neuropathy, Small cell lung carcinoma, Staphyloma posticum, Transient hyperphenylalaninemia, Tricuspid Valve Insufficiency, Trifunctional Protein Deficiency, Von Willebrand Disorder, Wilms tumor
|
205
|
|
|
HADHA pseudogene 1 |
HADHAP |
Curated: N/A
Unreviewed: N/A
|
206
|
|
|
HADHA pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
207
|
|
|
Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta |
ECHB, MSTP029, MTPB, MTPD, MTPD2, TP-BETA |
Curated: Breast neoplasms, Charcot-marie-tooth disease, Fatty liver, Fatty liver, alcoholic, Heart disease, Mitochondrial disease, Non-small cell lung carcinoma, Oligodendroglioma, Rickets, Trifunctional protein deficiency, mitochondrial trifunctional protein deficiency
Unreviewed: Abetalipoproteinemia, Adrenoleukodystrophy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiomyopathy, Carnitine palmitoyltransferase deficiency, Charcot-Marie-Tooth Disease, Cholestasis, Colorectal Cancer, Colorectal neoplasm, Congenital Clubfoot, Congestive Heart Failure, Deficiency Of Acetyl-CoA Acetyltransferase, Developmental Delay, Disorder Of Skeletal Muscle, Distal peripheral sensory neuropathy, Fatty Liver, Heart Diseases, Hereditary sensory and autonomic neuropathy, Hydrops Fetalis, Hypoparathyroidism, Ketosis, Learning Disorders, Left Ventricular Hypertrophy, Lipid Metabolism Disorders, Liver failure, Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Malignant Neoplasm, Mammary Neoplasms, Marfan Syndrome, Melanoma, Mitochondrial trifunctional protein deficiency, Motor delay, Myopathy, Neoplasms, Nervous System Diseases, Neuropathy, Non-Alcoholic Fatty Liver Disease, Peripheral axonal neuropathy, Polyneuropathy, Prostate adenocarcinoma, Prostate cancer, Prostatic neoplasm, Prostatitis, Respiratory Failure, Retinitis Pigmentosa, Sensorimotor neuropathy, Tricuspid Valve Insufficiency, Trifunctional Protein Deficiency, Urinary bladder neoplasms
|
208
|
|
|
HADHB pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
209
|
|
|
HuR (ELAVL1) associated fibroblast migratory lncRNA |
- |
Curated: N/A
Unreviewed: N/A
|
210
|
|
|
Hydroxyacylglutathione hydrolase |
GLO2, GLO2D, GLX2, GLXII, HAGH1 |
Curated: Glyoxalase ii deficiency, Schizophrenia
Unreviewed: Adenocarcinoma, Alzheimer disease, Autism Spectrum Disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Diabetes mellitus, Kidney Failure, Lung carcinoma, Neoplasms, Polycystic kidney disease, Prostate cancer, Prostatic Neoplasms, Renal Insufficiency, Rett Syndrome, Rheumatoid arthritis
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