|
911
|
|
|
DEAF1 transcription factor |
MRD24, NEDHELS, NUDR, SPN, VSVS, ZMYND5 |
Anxiety disorder, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Developmental dysplasia of the hip, Developmental delay, Developmental regression, Dwarfism, Dyskinesia, seizures, and intellectual developmental disorder, Dyskinetic syndrome, Dysmorphic features, Dyssomnia, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hypercholesterolemia, Hypothyroidism, Mental retardation, Intellectual disability-epilepsy-extrapyramidal syndrome, Low-frequency hearing loss, Macrocephaly, Malocclusion, Mental depression, Microcephaly, Microcornea, Micrognathism, Mood swings, Myopia, Non-syndromic intellectual disability, Obesity, Otitis media, Pica, Precocious puberty, Repetitive compulsive behavior, Retinal detachment, Scoliosis, Sleep disorders, Smith-magenis syndrome, Speech disorders, Status epilepticus, Stereotyped behavior, Strabismus, Syndactyly of the toes, Synophrys, TaurodontismView all (33 more) |
|
912
|
|
|
Lysine acetyltransferase 5 |
ESA1, HTATIP, HTATIP1, NEDFASB, PLIP, TIP, TIP60, ZC2HC5, cPLA2 |
|
|
913
|
|
|
Hypoxia up-regulated 1 |
GRP-170, Grp170, HSP12A, IMD59, ORP-150, ORP150 |
Agranulocytosis, Congenital pectus carinatum, Dwarfism, Encephalitis, Granulocytopenia with immunoglobulin abnormality, Hidradenitis suppurativa, High palate, Hypochromic anemia, Immunologic deficiency syndromes, Malabsorption syndrome, Micrognathism, Spinocerebellar ataxia, Stomatitis |
|
914
|
|
|
- |
BWS, H19-DMD, IC1, ICR1, ICR1-DMR, SRS1, WT2 |
Adrenocortical carcinoma, Beckwith-wiedemann syndrome, Cardiomyopathy, Congenital hemihypertrophy, Congenital omphalocele, Cryptorchidism, Gonadoblastoma, Hepatoblastoma, Macroglossia, Hypoglycemia, Nephroblastoma, Nephrocalcinosis, Nephrolithiasis, Phakomatosis pigmentovascularis, Proptosis, Vesicoureteral refluxView all (1 more) |
|
915
|
|
|
Importin 8 |
RANBP8, VISS |
|
|
916
|
|
|
NOP56 ribonucleoprotein |
NOL5A, SCA36 |
Spinocerebellar ataxia, Attention deficit hyperactivity disorder, Bowel incontinence, Cerebellar atrophy, Dysarthria, Dysphagia, Gastric cancer, Lung adenocarcinoma, Migraine, Nystagmus, Ptosis, Stomach neoplasms |
|
917
|
|
|
Nebulette |
C10orf113, LASP2, LNEBL, bA165O3.1 |
Atrial fibrillation, Cardiomyopathy, Coronary aneurysm, Dilated cardiomyopathy, Hearing loss, Hypertrophic cardiomyopathy, Kawasaki disease, Left ventricular hypertrophy, Lipoatrophy, Lipodystrophy, Myopathy, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Rheumatoid arthritis |
|
918
|
|
|
CCAAT enhancer binding protein epsilon |
C/EBP-epsilon, CRP1, IMD108, SGD1, c/EBP epsilon |
|
|
919
|
|
|
Pitrilysin metallopeptidase 1 |
MP1, PreP, SCAR30 |
|
|
920
|
|
|
Autophagy related 7 |
APG7-LIKE, APG7L, GSA7, SCAR31 |
|
