|
751
|
|
|
Ankyrin repeat domain 55 |
- |
Alzheimer disease, Ankylosing spondylitis, Apraxia, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Celiac disease, Cholangitis, Common variable immunodeficiency, Crohn disease, Diabetes mellitus, Immune system diseases, Inflammatory bowel disease, Iridocyclitis, Leukemia, Lupus erythematosus, Multiple sclerosis, Oligoarticular arthritis, Pauciarticular chronic arthritis, Polyarthritis, Seronegative polyarthritis, Psoriasis, Rheumatoid arthritis, Rheumatoid factor-negative polyarticular arthritis, Still disease, Stress disorder, Ulcerative colitisView all (12 more) |
|
752
|
|
|
Androglobin |
C6orf103, CAPN16 |
|
|
753
|
|
|
ALG9 alpha-1,2-mannosyltransferase |
CDG1L, DIBD1, GIKANIS, LOH11CR1J |
Brachycephaly, Cardiovascular diseases, Cerebellar atrophy, Congenital disorder of glycosylation, Congenital heart defects, Pulmonary hypoplasia, Cystic kidney disease, Cystic liver disease, Defect of skull ossification, Developmental delay, Epileptic encephalopathy, Esotropia, Frontal bossing, Heart septal defects, Impaired cognition, Liver failure, Macrostomia, Mental retardation, Mesatipellic pelvis, Microcephaly, Micrognathism, Osteochondrodysplasia, Pericardial effusion, Polycystic kidney disease, Polycystic kidney disease with microbrachycephaly, hypertelorism, and brachymelia, Polycystic liver disease, Posteriorly rotated ear, Proptosis, Skeletal dysplasiaView all (14 more) |
|
754
|
|
|
Armadillo repeat containing 5 |
AIMAH2 |
|
|
755
|
|
|
Rho GTPase activating protein 28 |
- |
|
|
756
|
|
|
Rho guanine nucleotide exchange factor 5 |
GEF5, P60, TIM, TIM1 |
|
|
757
|
|
|
AGBL carboxypeptidase 2 |
CCP2 |
|
|
758
|
|
|
ALG13 UDP-N-acetylglucosaminyltransferase subunit |
CDG1S, CXorf45, DEE36, EIEE36, GLT28D1, MDS031, TDRD13, YGL047W |
Attention deficit hyperactivity disorder, Autism, Brachycephaly, Brain atrophy, Cerebral atrophy, Cerebral cortical atrophy, Congenital disorder of glycosylation, Developmental delay, Epilepsy, Epileptic encephalopathy, Facial paralysis, Neurosensory hearing impairment, Horizontal nystagmus, Impaired cognition, Infantile spasms, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Microcephaly, Micrognathism, Neurodevelopmental disorders, Non-syndromic intellectual disability, x-linked, Nystagmus, Obesity, Optic atrophy, Osteopenia, Seizure, Syndactyly of the toes, West syndromeView all (15 more) |
|
759
|
|
|
Actin related protein 5 |
Arp5, INO80M |
|
|
760
|
|
|
ATPase family AAA domain containing 5 |
C17orf41, ELG1, FRAG1 |
|
