381
|
|
|
Acyl-CoA dehydrogenase family member 8 |
ACAD-8, ARC42, IBDH |
|
382
|
|
|
Ankyrin repeat domain 1 |
ALRP, C-193, CARP, CVARP, MCARP, bA320F15.2 |
Cardiomyopathy, Congenital total pulmonary venous return anomaly, Dilated cardiomyopathy, Endometrioma, Endometriosis, Hearing loss, Hypertrophic cardiomyopathy, Lipoatrophy, Lipodystrophy, Myopathy, Palmoplantar keratoderma |
383
|
|
|
Adenosine monophosphate deaminase 2 |
AMPD, PCH9, SPG63 |
Central visual impairment, Cerebral cortical atrophy, Brain malformation, Developmental delay, Dwarfism, Epilepsy, Hypoplasia of corpus callosum, Macroglossia, Optic atrophy, Peripheral axonal neuropathy, Pontoneocerebellar hypoplasia, Spastic paraplegia |
384
|
|
|
ALF transcription elongation factor 4 |
AF5Q31, CHOPS, MCEF |
Bone disease, Brachydactyly, Chops syndrome, Cognitive disorder, Congenital heart defects, Cryptorchidism, Developmental delay, Dwarfism, Gastroesophageal reflux disease, Heart septal defects, Laryngomalacia, Leukemia, Lung diseases, Mental retardation, Multiple congenital anomalies, Obesity, Patent ductus arteriosus, Proptosis, Tracheal stenosis, Vesicoureteral refluxView all (5 more) |
385
|
|
|
Argonaute RISC catalytic component 2 |
CASC7, EIF2C2, LESKRES, LINC00980, PPD, Q10 |
|
386
|
|
|
Adenosine monophosphate deaminase 3 |
- |
|
387
|
|
|
AT-hook DNA binding motif containing 1 |
MRD25, XIGIS |
Metabolic syndrome, Developmental delay, Esotropia, Hypoplasia of corpus callosum, Mental retardation, Intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome, Laryngomalacia, Micrognathism, Hypotonia, Sleep apnea, Submucosal cleft palate, Xia-gibbs syndrome |
388
|
|
|
Amphiphysin |
AMPH1 |
|
389
|
|
|
Angiopoietin like 3 |
ANG-5, ANGPT5, ANL3, FHBL2 |
|
390
|
|
|
Apolipoprotein B mRNA editing enzyme catalytic subunit 3C |
A3C, APOBEC1L, ARDC2, ARDC4, ARP5, PBI, bK150C2.3 |
|