|
591
|
|
|
Muscle associated receptor tyrosine kinase |
CMS9, FADS, FADS1 |
Absence of septum pellucidum, Akinesia, Amyotrophy, Elbow ankylosis, Arthrogryposis multiplex congenita, Blepharophimosis, Cerebellar hypoplasia, Congenital clubfoot, Pulmonary hypoplasia, Myasthenic syndrome, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Facial paralysis, Fetal akinesia deformation sequence, High palate, Hydrocephalus, Cystic hygroma, Micrognathism, Microstomia, Myasthenia gravis, Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency, Myasthenic syndrome, congenital, with facial dysmorphism, associated with acetylcholine receptor deficiency, Hypotonia, Pena shokeir syndrome, Posteriorly rotated ear, Proptosis, Pterygium, Ptosis, Respiratory failure, Scoliosis, Thoracic hypoplasia, Vertical talusView all (18 more) |
|
592
|
|
|
Methylmalonyl-CoA mutase |
MCM, MUT |
Anemia, Anorexia, Atrial septal defect, Cardiomyopathy, Choreoathetosis, Developmental delay, Dysarthria, Hemiplegia/hemiparesis, Immunologic deficiency syndromes, Inborn errors of metabolism, Kidney disease, Leukopenia, Mental retardation, Methylmalonic aciduria, Nephritis, Neutropenia, Obesity, Optic atrophy, Pancreatitis, Renal insufficiency, Renal tubular disorder, Stroke, SyndactylyView all (8 more) |
|
593
|
|
|
MutY DNA glycosylase |
MYH |
Adenocarcinoma of colon, Adenomatous polyposis, B lymphoblastic leukemia lymphoma, Benign neoplasm of stomach, Breast cancer, Hereditary cancer syndrome, Colon carcinoma, Colonic neoplasms, Colorectal adenomatous polyposis, Colorectal cancer, Endometrial carcinoma, Multiple polyposis syndrome, Gastric cancer, Intestinal carcinoid, Intestinal polyposis, Polyposis, Ovarian cancer, Pilomatrixoma, Polyp of large intestine, Prostate cancer, Rectal polyp, Skin neoplasms, Stomach neoplasms, Stomach carcinomaView all (9 more) |
|
594
|
|
|
Mevalonate diphosphate decarboxylase |
FP17780, MDDase, MPD, POROK7 |
|
|
595
|
|
|
Mevalonate kinase |
LRBP, MK, MVLK, POROK3 |
Aphthous ulcer, Arthritis, Autoinflammatory disease, Carcinoma, Cataract, Cerebellar ataxia, Cerebellar atrophy, Cerebellar vermis agenesis, Cerebral atrophy, Cerebral cortical atrophy, Deficiency of mevalonate kinase, Developmental delay, Disseminated superficial actinic porokeratosis, Dolichocephaly, Dwarfism, Hyperimmunoglobulinemia, Hyperkeratosis, Hypoplastic anemia, Intestinal obstruction, Liver carcinoma, Mental retardation, Methylmalonic aciduria, Microcephaly, Migraine, Neutrophilia, Nyctalopia, Nystagmus, Parakeratosis, Polyarthralgia, Porokeratosis, Posteriorly rotated ear, Rod-cone dystrophy, Urticaria, VasculitisView all (19 more) |
|
596
|
|
|
MX dynamin like GTPase 1 |
IFI-78K, IFI78, MX, MxA, lncMX1-215 |
|
|
597
|
|
|
MX dynamin like GTPase 2 |
MXB |
|
|
598
|
|
|
MAX interactor 1, dimerization protein |
MAD2, MXD2, MXI, bHLHc11 |
|
|
599
|
|
|
MYB proto-oncogene, transcription factor |
Cmyb, c-myb, c-myb_CDS, efg |
|
|
600
|
|
|
MYB proto-oncogene like 1 |
A-MYB, AMYB |
|
