|
211
|
|
|
Aristaless related homeobox |
CT121, EIEE1, ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRX76, MRX87, MRXS1, PRTS |
Agenesis of corpus callosum, Ambiguous genitalia, Attention deficit hyperactivity disorder, Autism, Cerebellar atrophy, Cerebral cortical atrophy, Choreoathetosis, Clonic seizures, Congenital exomphalos, Congenital hypoplasia of penis, Corpus callosum agenesis-abnormal genitalia syndrome, Cryptorchidism, Developmental delay, Developmental regression, Duane retraction syndrome, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysmorphic features, Dysphagia, Dyssomnia, Epileptic encephalopathy, Epileptic-dyskinetic encephalopathy, Episodic ataxia, Exocrine pancreatic insufficiency, Facial paralysis, Febrile seizures, Focal dystonia, Focal seizures, Neurosensory hearing impairment, High palate, Hirschsprung disease, Hydranencephaly and abnormal genitalia, Hypohidrosis, Hypoplasia of corpus callosum, Hypospadias, Hypotonic seizures, Mental retardation, Lissencephaly, x-linked, Macrocephaly, Malabsorption syndrome, Meckel diverticulum, Mental retardation, x-linked, Microcephaly, Micrognathism, Myoclonic seizures, Hypotonia, Non-syndromic intellectual disability, x-linked, Nystagmus, Obesity, Optic atrophy, Pachygyria, Partington syndrome, Patent ductus arteriosus, Penis agenesis, Precocious puberty, Quadriplegia, Renal dysplasia, Scoliosis, Seizure, Sleep disorders, Spasms syndrome, Spasms x-linked, Spastic quadriplegia, Spasticity-intellectual disability-epilepsy syndrome, x-linked, Specific learning disorder, Status epilepticus, Strabismus, Syndactyly of the toes, Synophrys, Ureterocele, Ventricular septal defect, West syndromeView all (58 more) |
|
212
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 15 |
DA12 |
|
|
213
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 16 |
ADAMTS16s |
|
|
214
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 17 |
WMS4 |
Carpal tunnel syndrome, Dwarfism, Ectopia lentis, Glaucoma, Ichthyosis-short stature-brachydactyly-microspherophakia syndrome, Iridodonesis, Liver neoplasms, Liver cancer, Myopia, Ocular hypertension, Osteosarcoma, Phacodonesis, Weill-marchesani syndrome |
|
215
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 18 |
ADAMTS21, KNO2, MMCAT |
|
|
216
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 19 |
CVDP2 |
|
|
217
|
|
|
ASXL transcriptional regulator 1 |
BOPS, MDS |
Accessory nipple, Agenesis of corpus callosum, Atrial septal defect, Bohring-opitz syndrome, Cerebral cortical atrophy, Congenital camptodactyly, Dislocated radial head, Congenital malrotation of intestine, Dandy-walker syndrome, Developmental delay, Dwarfism, Dysmorphic features, Eosinophilia, Gastroesophageal reflux disease, Glabellar hemangioma, High palate, Hydronephrosis, Hypertrichosis, Hypoplasia of corpus callosum, Mental retardation, Intestinal volvulus, Leukemia, Non-hodgkin lymphoma, Mastocytosis, Microcephaly, Micrognathism, Microtia, Movement disorders, Multicystic renal dysplasia, Multiple congenital anomalies, Myelodysplasia, Myelodysplastic syndrome, Myeloid leukemia, Myelomonocytic leukemia, Myopia, Nephroblastoma, Neuronal heterotopia, Patent foramen ovale, Phakomatosis pigmentovascularis, Posteriorly rotated ear, Promyelocytic leukemia, Proptosis, Retinal diseases, Scoliosis, Sleep apnea, Spade-like hand, Spastic quadriplegia, Strabismus, Syndactyly, Synophrys, Systemic mastocytosis, Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease, Systemic mastocytosis with associated hematologic neoplasm, Talipes, Trigonocephaly, Ventricular septal defect, Vesicoureteral reflux, Wilms tumorView all (43 more) |
|
218
|
|
|
AFG3 like matrix AAA peptidase subunit 1, pseudogene |
AFG3, AFG3L1 |
|
|
219
|
|
|
Afamin |
ALB2, ALBA, ALF |
|
|
220
|
|
|
Alpha fetoprotein |
AFPD, FETA, HPAFP |
|
