|
2681
|
|
|
Dihydrofolate reductase |
DHFR1, DHFRP1, DYR |
Anemia, Autism, Breast cancer, Mammary neoplasms, Breast carcinoma, Cerebellar hypoplasia, Cerebral atrophy, Colorectal cancer, Colorectal neoplasms, Constitutional megaloblastic anemia with severe neurologic disease, Deficiency of dihydrofolate reductase, Developmental delay, Folic acid deficiency, Inborn errors of metabolism, Marfan syndrome, Megaloblastic anemia, Miscarriage, Nervous system disorder, Osteosarcoma, Pancytopenia, Rheumatoid arthritis, SubfertilityView all (7 more) |
|
2682
|
|
|
AFG3 like matrix AAA peptidase subunit 1, pseudogene |
AFG3, AFG3L1 |
|
|
2683
|
|
|
Dihydroorotate dehydrogenase (quinone) |
DHOdehase, POADS, URA1 |
Abnormal dermatoglyphic pattern, Accessory nipple, Anemia, Beta thalassemia, Choanal atresia, Developmental dysplasia of the hip, Congenital hypoplasia of radius, Congenital pectus excavatum, Cooley`s anemia, Cryptorchidism, Ectropion, Erythroblastic leukemia, Hearing loss, Hemoglobinopathy, Hereditary spherocytosis, Hypoplasia of thumb, Micrognathism, Microtia, Miller syndrome, Multicystic renal dysplasia, Narcolepsy, Peg-shaped teeth, Penis agenesis, Radioulnar synostosis, Strabismus, Supernumerary vertebra, Syndactyly, Syndactyly of fingers, ThalassemiaView all (14 more) |
|
2684
|
|
|
Deoxyhypusine synthase |
DHS, DS, MIG13, NEDSSWI |
|
|
2685
|
|
|
Cytochrome b5 reductase 3 |
B5R, DIA1 |
Cerebellar atrophy, Congenital methemoglobinemia, Developmental delay, Esotropia, Hereditary methemoglobinemia, Mental retardation, Methemoglobinemia, Microcephaly, Nadh-cytochrome b5 reductase deficiency, Polycythemia, Spastic quadriplegia, Strabismus, Temporal cortical atrophy |
|
2686
|
|
|
NAD(P)H quinone dehydrogenase 1 |
DHQU, DIA4, DTD, NMOR1, NMORI, QR1 |
Asthma, Benign neoplasm, Urinary bladder cancer, Bladder neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Cholestasis, Colorectal cancer, Colorectal neoplasms, Dermatitis, Hemolytic uremic syndrome, Hyperglycemia, Kidney disease, Kidney failure, Lymphoblastic leukemia, Lung carcinoma, Malignant neoplasm, Marfan syndrome, Monocytic leukemia, Multiple myeloma, Myeloid leukemia, Neoplasms, Non-alcoholic fatty liver disease, Obesity, Papilloma, Papillomatosis, Parkinson disease, Prostatic neoplasms, Prostate cancer, Acute kidney insufficiency, Spinocerebellar ataxiaView all (17 more) |
|
2687
|
|
|
Diaphanous related formin 1 |
DFNA1, DIA1, DRF1, LFHL1, SCBMS, hDIA1, mDia1 |
Central visual impairment, Deafness, Developmental delay, Dwarfism, Eczema, Epilepsy, Hearing loss, Hypoplasia of corpus callosum, Low-frequency hearing loss, Mental retardation, Microcephaly, Optic atrophy, Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome, Seizures, cortical blindness, and microcephaly syndrome, Sensorineural hearing loss-thrombocytopenia syndrome |
|
2688
|
|
|
Afamin |
ALB2, ALBA, ALF |
|
|
2689
|
|
|
Diaphanous related formin 2 |
DIA, DIA2, DRF2, POF, POF2, POF2A |
|
|
2690
|
|
|
Iodothyronine deiodinase 1 |
5DI, THMA2, TXDI1 |
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