|
731
|
|
|
Actin alpha cardiac muscle 1 |
ACTC, ASD5, CMD1R, CMH11, LVNC4 |
Ametropia, Atrial septal defect, Cardiomyopathy, Congestive heart failure, Dilated cardiomyopathy, Gastric cancer, Hearing loss, Hypertrophic cardiomyopathy, Left ventricular noncompaction, Lipoatrophy, Lipodystrophy, Multiple congenital anomalies, Myopathy, Palmoplantar keratoderma, Secundum atrial septal defect, Stomach neoplasms, Wolff-parkinson-white syndromeView all (2 more) |
|
732
|
|
|
Actin gamma 1 |
ACT, ACTG, DFNA20, DFNA26, HEL-176 |
Anaplastic carcinoma, Anencephaly, Aphasia, Baraitser-winter syndrome, Carcinoma, Cerebral cortical hemiatrophy, Coloboma of eye, Coloboma of optic disc, Congenital coloboma of iris, Congenital epicanthus, Congenital euryblepharon, Congenital ocular coloboma, Coronary syndrome, Deafness, Developmental delay, Drachtman weinblatt sitarz syndrome, Dysmorphic features, Dysphasia, Epilepsy, Hydronephrosis, Lissencephaly, Macrostomia, Mental retardation, Microcephaly, Microcornea, Micrognathism, Multiple congenital anomalies, Neck webbing, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Osteochondrodysplasia, Osteochondrosis, Osteoporosis, Pachygyria, Polymicrogyria, Ptosis, Retinoschisis, Scoliosis, Sensorineural hearing loss, Skeletal dysplasia, Specific learning disorder, Subcortical cerebral atrophy, Transient ischemic attack, Trigonocephaly, Uveoretinal colobomaView all (30 more) |
|
733
|
|
|
Actin gamma 2, smooth muscle |
ACT, ACTA3, ACTE, ACTL3, ACTSG, MMIHS5, VSCM, VSCM1 |
Anonychia, Arachnodactyly, Berdon syndrome, Cardiac neoplasms, Colonic neoplasms, Congenital exomphalos, Congenital malrotation of intestine, Congenital omphalocele, Cryptorchidism, Dysphagia, Hirschsprung disease, Hydronephrosis, Hyperparathyroidism, Intestinal pseudoobstruction, Malnutrition, Megacystis-microcolon-intestinal hypoperistalsis syndrome, Microcephaly, Microcolon, Micrognathism, Multicystic renal dysplasia, Multiple congenital anomalies, Myopathic intestinal pseudoobstruction, Situs inversus, Vesicoureteral reflux, Visceral myopathy, Visceral neuropathyView all (11 more) |
|
734
|
|
|
Ataxin 8 |
- |
|
|
735
|
|
|
AGBL1 antisense RNA 1 |
- |
|
|
736
|
|
|
Adenosylmethionine decarboxylase 1 pseudogene 3 |
- |
|
|
737
|
|
|
ALMS1 centrosome and basal body associated protein |
ALSS |
Acanthosis nigricans, Alopecia, Alstrom syndrome, Asthma, Atherosclerosis, Autism, Bardet-biedl syndrome, Cardiomyopathy, Cataract, Cirrhosis, Cone-rod dystrophy, Congestive heart failure, Developmental delay, Diabetes insipidus, Diabetes mellitus, Disorder of eye, Dwarfism, Fatty liver, Gingivitis, Gynecomastia, Hyperinsulinism, Hyperostosis of skull, Hypertension, Hyperuricemia, Hypogonadism, Hypothyroidism, Insulin-resistant diabetes mellitus, Isolated somatotropin deficiency, Kidney disease, Leukodystrophy, Liver failure, Mental depression, Mental retardation, Multinodular goiter, Nephritis, Nephrocalcinosis, Nystagmus, Obesity, Obsessive-compulsive disorder, Otitis media, Polycystic ovary syndrome, Polydactyly, Portal hypertension, Precocious puberty, Pulmonary arterial hypertension, Pulmonary fibrosis, Renal glomerular disease, Renal insufficiency, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Schizophrenia, Scoliosis, Somatotropin deficiency, Subcapsular cataract, Testicular hypogonadism, Vesicoureteral refluxView all (42 more) |
|
738
|
|
|
AHNAK nucleoprotein |
AHNAK1, AHNAKRS, PM227 |
|
|
739
|
|
|
ALG8 alpha-1,3-glucosyltransferase |
CDG1H, PCLD3 |
Anemia, Cataract, Cholestasis, Congenital camptodactyly, Congenital clubfoot, Congenital disorder of glycosylation, Cryptorchidism, Cystic kidney disease, Cystic liver disease, Heart septal defects, Hypoalbuminemia, Hypothyroidism, Liver cyst, Liver failure, Macroglossia, Mental depression, Micrognathism, Patent ductus arteriosus, Polycystic liver disease, Protein-losing enteropathy, Renal cystView all (6 more) |
|
740
|
|
|
ASPSCR1 tether for SLC2A4, UBX domain containing |
ASPCR1, ASPL, ASPS, RCC17, TUG, UBXD9, UBXN9 |
|
