|
471
|
|
|
A-Raf proto-oncogene, serine/threonine kinase |
A-RAF, ARAF1, PKS2, RAFA1 |
|
|
472
|
|
|
Acyl-CoA dehydrogenase very long chain |
ACAD6, LCACD, VLCAD |
Acyl coa dehydrogenase deficiency, Atrioventricular block, Cardiomyopathy, Dermatitis, Fatty liver, Hypertrophic cardiomyopathy, Hypoproteinemia, Macrocephaly, Metabolic myopathy, Myopathy, Obesity, Patent foramen ovale, Pearson`s marrow-pancreas syndrome, Pericardial effusion, Ventricular fibrillation, Ventricular septal defect, Ventricular tachycardiaView all (2 more) |
|
473
|
|
|
Archain 1 coat protein complex I subunit delta |
COPD, SRMMD, SSMG |
Astigmatism, High palate, Hypospadias, Mental retardation, Microcephaly, Micrognathism, Motor delay, Myopia, Penis agenesis, Rhizomelia, Rubral tremor, Scaphocephaly, Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay, Sleep apnea, Syndactyly of the toes, Ventricular septal defectView all (1 more) |
|
474
|
|
|
Anosmin 1 |
ADMLX, HH1, HHA, KAL, KAL1, KALIG-1, KMS, WFDC19 |
Anxiety disorder, Azoospermia, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dysarthria, Dysmorphic features, Erectile dysfunction, Female hypogonadism syndrome, Gynecomastia, Hearing loss, High palate, Hypogonadotropic hypogonadism, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Multiple congenital anomalies, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Renal aplasia, Renal glomerular disease, Secondary physiologic amenorrhea, Skeletal dysplasia, Testicular atrophy, Testicular hypogonadismView all (24 more) |
|
475
|
|
|
Amphiregulin |
AR, AREGB, CRDGF, SDGF |
Alveolitis, Arthritis, Asthma, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Endometrioma, Endometriosis, Erythropoietic protoporphyria, Ferrochelatase deficiency, Gastric cancer, Head and neck neoplasms, Head neoplasms, Neck cancer, Neoplasm of head, Juvenile arthritis, Lung carcinoma, Head and neck cancer, Marfan syndrome, Myocardial ischemia, Neck neoplasms, Ovarian neoplasm, Ovarian cancer, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Pulmonary fibrosis, Still disease, Stomach neoplasms, Upper aerodigestive tract neoplasmsView all (15 more) |
|
476
|
|
|
Asparaginase |
C14orf76, GPA/WT, LYSOLP, hASNase1 |
|
|
477
|
|
|
ATPase phospholipid transporting 9B (putative) |
ATPASEP, ATPIIB, HUSSY-20, NEO1L, hMMR1 |
|
|
478
|
|
|
ARF GTPase 1 |
PVNH8 |
Aortic aneurysm, Aortic valve insufficiency, Attention deficit hyperactivity disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Gastroesophageal reflux disease, Marfan syndrome, Patent ductus arteriosus, Periventricular nodular heterotopia, Scoliosis |
|
479
|
|
|
Agrin |
AGRIN, CMS8, CMSPPD |
Acquired kyphoscoliosis, Arthrogryposis multiplex congenita, Bulbar palsy, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Developmental delay, Distal amyotrophy, Dysphagia, Esotropia, Facial paralysis, Gastroesophageal reflux disease, Hearing loss, High palate, Leukemia, Mental retardation, Motor delay, Myasthenia gravis, Myeloid leukemia, Nystagmus, Polyneuropathy, Ptosis, Respiratory failure, Sleep apnea, Sudden episodic apneaView all (11 more) |
|
480
|
|
|
Acetyl-CoA acetyltransferase 1 |
ACAT, MAT, T2, THIL |
Anorexia, Beta-ketothiolase deficiency, Clonic seizures, Deficiency of acetyl-coa acetyltransferase, Extrapyramidal dyskinesia, Hyperglycemia, Hypertension, Hyperuricemia, Hypoglycemia, Hypotonic seizures, Mental retardation, Jacksonian seizure, Ketonuria, Ketosis, Kidney failure, Motor delay, Oral aversion, Seizure, ThrombocytosisView all (4 more) |
