|
331
|
|
|
Eukaryotic translation initiation factor 4 gamma 3 |
eIF-4G 3, eIF4G 3, eIF4GII |
|
|
332
|
|
|
Embryonic ectoderm development |
COGIS, HEED, WAIT1 |
Cataract, Cohen-gibson syndrome, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Dysplastic corpus callosum, Hyperopia, Macrocephaly, Macrotia, Melanocytic nevus, Mental retardation, Micrognathism, Myopia, Nerve sheath tumors, Neurilemmoma, Peripheral nerve sheath neoplasm, Osteopenia, Perineurioma, Ptosis, Schwannomatosis, Scoliosis, Syndactyly of fingers, Synophrys, Talipes transversoplanus, Weaver syndromeView all (14 more) |
|
333
|
|
|
Eukaryotic translation initiation factor 2B subunit delta |
EIF-2B, EIF2B, EIF2Bdelta, VWM4 |
Cach syndrome, Central nervous system demyelination, Cree leukoencephalopathy, Delusions, Developmental regression, Dysarthria, Leukoencephalopathy, Leukoencephalopathy with vanishing white matter, Lung adenocarcinoma, Macrocephaly, Mood swings, Optic atrophy, Ovarioleukodystrophy, Physiologic amenorrhea, Premature menopause, Secondary physiologic amenorrheaView all (1 more) |
|
334
|
|
|
Eukaryotic translation initiation factor 2B subunit gamma |
EIF-2B, EIF2Bgamma, VWM3 |
Cach syndrome, Central nervous system demyelination, Cree leukoencephalopathy, Delusions, Developmental regression, Dysarthria, Leukoencephalopathy, Leukoencephalopathy with vanishing white matter, Macrocephaly, Mood swings, Optic atrophy, Ovarioleukodystrophy, Physiologic amenorrhea, Premature menopause, Secondary physiologic amenorrhea |
|
335
|
|
|
Eukaryotic translation initiation factor 2B subunit beta |
EIF-2Bbeta, EIF2B, EIF2Bbeta, VWM2 |
Cach syndrome, Central nervous system demyelination, Cree leukoencephalopathy, Delusions, Developmental regression, Dysarthria, Leukoencephalopathy, Leukoencephalopathy with vanishing white matter, Macrocephaly, Mood swings, Optic atrophy, Ovarioleukodystrophy, Physiologic amenorrhea, Premature menopause, Secondary physiologic amenorrhea |
|
336
|
|
|
Eukaryotic translation initiation factor 2B subunit epsilon |
CACH, CLE, EIF-2B, EIF2Bepsilon, LVWM, VWM5 |
Cach syndrome, Central nervous system demyelination, Cerebellar ataxia, Cree leukoencephalopathy, Delusions, Developmental regression, Dysarthria, Impaired cognition, Leukodystrophy, Leukoencephalopathy, Leukoencephalopathy with vanishing white matter, Lung adenocarcinoma, Macrocephaly, Mood swings, Movement disorders, Optic atrophy, Ovarioleukodystrophy, Physiologic amenorrhea, Premature menopause, Secondary physiologic amenorrheaView all (5 more) |
|
337
|
|
|
Eukaryotic translation initiation factor 2 subunit beta |
EIF2, EIF2B, EIF2beta, PPP1R67, eIF-2-beta |
|
|
338
|
|
|
EF-hand calcium binding domain 11 |
C14orf143 |
|
|
339
|
|
|
Expanded repeat domain, CAG/CTG 1 |
- |
|
|
340
|
|
|
Exocyst complex component 3 like 2 |
BMRS, XTP7 |
Alzheimer disease, Anhydramnios, Coronary artery disease, Dandy-walker syndrome, Exudative macular degeneration, Geographic atrophy, Hydrocephalus, Age-related macular degeneration, Meckel-gruber syndrome, Pancytopenia, Polycystic kidney disease, Renal dysplasia |
