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1
|
|
|
Wound and keratinocyte migration associated lncRNA 2 |
lnc-TNFAIP3 |
|
|
2
|
|
|
WTAP pseudogene 1 |
- |
|
|
3
|
|
|
WARS2 antisense RNA 1 |
- |
|
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4
|
|
|
Tryptophanyl tRNA synthetase 2, mitochondrial |
NEMMLAS, PKDYS3, TrpRS, mtTrpRS |
Absence of septum pellucidum, Alopecia, Autism, Central visual impairment, Cerebellar atrophy, Cerebral atrophy, Combined oxidative phosphorylation deficiency, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Exotropia, Hypoglycemia, Hypoplasia of corpus callosum, Mental retardation, Liver failure, Mental depression, Microcephaly, Motor delay, Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures, Nystagmus, Optic atrophy, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Spastic quadriplegia, Stereotyped behaviorView all (13 more) |
|
5
|
|
|
WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit |
GAMOS6, MIGSB, TRM82, TRMT82, Wuho, hWH |
Aqueductal stenosis, Camptodactyly of fingers, Congenital epicanthus, Developmental delay, Dwarfism, Dyssomnia, Galloway-mowat syndrome, Hemiplegia/hemiparesis, Hiatal hernia, High palate, Impaired cognition, Kidney disease, Macrostomia, Macrotia, Mental retardation, Microcephaly, Microdontia, Micrognathism, Myeloproliferative disorder, Nephrotic syndrome, Optic atrophy, Pachygyria, Partial agenesis of corpus callosum, Pituitary dwarfism, Proptosis, Seckel syndrome, Sleep disordersView all (12 more) |
|
6
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|
|
WASP family member 3 |
Brush-1, SCAR3, WAVE3 |
|
|
7
|
|
|
WW domain containing E3 ubiquitin protein ligase 2 |
AIP2, WWp2-like |
|
|
8
|
|
|
WD repeat domain 45 |
JM5, NBIA4, NBIA5, WDRX1, WIPI-4, WIPI4 |
Beta-propeller protein-associated neurodegeneration, Cerebellar atrophy, Cerebral atrophy, Cerebral, cerebellar, coloboma syndrome, x-linked, Dementia, Developmental delay, Dysautonomia, Dysmorphic features, Dyssomnia, Epilepsy, Heart failure, Hypoplasia of corpus callosum, Infantile spasms, Mental retardation, Movement disorders, Multiple congenital anomalies, Nephropathy with pretibial epidermolysis bullosa and deafness, Neurodegeneration with brain iron accumulation, Neurodevelopmental disorders, Optic atrophy, Parkinson disease, Sleep disorders, Spasms syndrome, West syndromeView all (9 more) |
|
9
|
|
|
WW domain binding protein 4 |
FBP21, NEDHFDB |
|
|
10
|
|
|
Wnt inhibitory factor 1 |
WIF-1 |
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