671
|
|
|
AFG3 like matrix AAA peptidase subunit 2 |
OPA12, SCA28, SPAX5 |
Curated: Spinocerebellar ataxia, Cerebellar ataxia, Central nervous system cancer, Chorea, Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome, Glioblastoma, Glioma, Glycogen storage disease, Hyperkinesia, Intellectual developmental disorder, Optic atrophy, Retinitis pigmentosa, Hearing loss, Spastic ataxia, AFG3L2-related optic atrophy and/or spastic ataxia spectrum
Unreviewed: Action Myoclonus-Renal Failure Syndrome, Amyotrophic lateral sclerosis, Ataxia, Ataxia, sensory, autosomal dominant, Basal ganglia disease, Cardiovascular disease, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar Diseases, Cerebellar Hypoplasia, Coronary artery disease, Demyelinating neuropathy, Dentatorubral Pallidoluysian Atrophy, Distal amyotrophy, Dysarthria, Dysphagia, Hemiplegia/hemiparesis, Henoch-Schonlein Nephritis, Hereditary spastic paraplegia, Hiatal Hernia, Hypercalcemia, Hypertension, Inclusion-Body Disease, Keratoconjunctivitis Sicca, Macular Degeneration, May-White Syndrome, Mental Depression, Mental retardation, MERRF Syndrome, Microcephaly, Mitochondrial Diseases, Myoclonic Epilepsy, Myoclonic Seizures, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Osteopenia, Parkinson Disease, Parotitis, Peripheral axonal neuropathy, Progressive External Ophthalmoplegia, Ptosis, Secondary parkinson disease, Seizure, Sensorimotor neuropathy, Sleep deprivation, Spastic Ataxia, Spastic Ataxia-Myoclonic Epilepsy-Neuropathy Syndrome, Spastic paraplegia, Spinocerebellar Ataxia, Vitamin D Deficiency
|
672
|
|
|
AFG3L2 pseudogene 1 |
AFG3L2P |
Curated: N/A
Unreviewed: N/A
|
673
|
|
|
Afamin |
ALB2, ALBA, ALF |
Curated: Kidney failure, Prostate cancer
Unreviewed: Acute Kidney Insufficiency, Adrenoleukodystrophy, Alcoholic Liver Cirrhosis, Alzheimer disease, Asthma, Blood Coagulation Disorders, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cataract, Chronic obstructive pulmonary disease, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Eclampsia, Endocrine system disease, Epilepsy, Epileptic encephalopathy, Esophageal varix, Fabry disease, Fatty liver, Fragile X syndrome, Fulminant Hepatitis, Gestational diabetes, Heart failure, Hepatolenticular Degeneration, Hermaphroditism, Hyperlipoproteinemia, Kidney Disease, Kidney Failure, Leukemia, Lewy Body Disease, Liver carcinoma, Liver Cirrhosis, Liver failure, Liver neoplasms, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Medulloblastoma, Melanoma, Metabolic Diseases, Metabolic Syndrome, Mitochondrial disease, Neoplasms, Obesity, Optic Atrophy, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian Failure, Ovarian neoplasm, Papillary thyroid cancer, Papillary thyroid carcinoma, Parkinson disease, Polycystic Ovary Syndrome, Schizophrenia, Sepsis, Squamous cell carcinoma, Teratozoospermia, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Ulcerative colitis
|
674
|
|
|
Arylformamidase |
FKF, KF, KFA |
Curated: Diverticular disease
Unreviewed: Amyotrophic lateral sclerosis, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Leiomyoma
|
675
|
|
|
Alpha fetoprotein |
AFPD, FETA, HPAFP |
Curated: Breast neoplasms, Hepatocellular carcinoma, Congenital alpha-fetoprotein deficiency, Liver disease, Premature ovarian failure, Stomach neoplasms
Unreviewed: N/A
|
676
|
|
|
Aftiphilin |
Nbla10388 |
Curated: N/A
Unreviewed: Inflammatory Bowel Disease, Ulcerative colitis
|
677
|
|
|
AFTPH divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
678
|
|
|
Aspartylglucosaminidase |
AGU, ASRG, GA |
Curated: Autism, Desbuquois syndrome, Intellectual developmental disorder, Neurodevelopmental disorder, Schizophrenia, aspartylglucosaminuria
Unreviewed: Achalasia, Acne, Alopecia, Alopecia, Male Pattern, Androgenetic Alopecia, Arthritis, Aspartylglucosaminuria, Attention Deficit Hyperactivity Disorder, Brachycephaly, Breast neoplasm, Cataract, Celiac disease, Cerebral Atrophy, Cholecystitis, Cirrhosis, Colorectal neoplasm, Congenital disorder of glycosylation, Congenital Exomphalos, Congenital Pectus Carinatum, Developmental regression, Diabetes, Diabetes Mellitus, Down Syndrome, Dwarfism, Dyskinetic Syndrome, Dyssomnia, Encephalitis, Eosinophilia, Esophageal Diseases, Fabry disease, Hypoparathyroidism, Inflammatory Bowel Disease, Irritable Bowel Syndrome, Liver carcinoma, Liver Cirrhosis, Lupus Nephritis, Macroglossia, Macrostomia, Malabsorption Syndrome, Malocclusion, Mental retardation, Metabolic Syndrome, Microcephaly, Microtia, Multiple Sclerosis, Neoplasms, Neutropenia, Otitis media, Pfaundler-Hurler Syndrome, Schizoaffective Disorder, Sclerosing Cholangitis, Scoliosis, Selective Immunoglobulin A Deficiency, Skin Diseases, Vascular, Sleep Disorders, Speech Disorders, Spondylolisthesis, Spondylolysis, Stomach Carcinoma, Stomach Neoplasms, Thyroid Diseases, Ulcerative colitis
|
679
|
|
|
AGA divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
680
|
|
|
- |
- |
Curated: N/A
Unreviewed: Osteogenesis Imperfecta
|