|
161
|
|
|
Dynein cytoplasmic 1 heavy chain 1 |
CDCBM13, CMT2O, DHC1, DHC1a, DNCH1, DNCL, DNECL, DYHC, Dnchc1, HL-3, SMALED1, p22 |
Nonmedullary thyroid carcinoma, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Cataract, Charcot-marie-tooth disease, Congenital epicanthus, Congenital microcephaly, Congenital pes cavus, Cortical dysplasia, Developmental delay, Distal lower limb amyotrophy, Dolichocephaly, Dysmorphic features, Dysphagia, Dysplastic corpus callosum, Hereditary motor and sensory neuropathy, Hereditary motor neuropathy, Congenital hip dislocation, Infantile spasms, Mental retardation, Malformation of cortical development, Microcephaly, Microlissencephaly, Motor delay, Myopathy, Non-syndromic intellectual disability, Pachygyria, Papillary thyroid carcinoma, Spinal muscular atrophy, Plagiocephaly, Polymicrogyria, Strabismus, Thyroid cancerView all (18 more) |
|
162
|
|
|
Dynein cytoplasmic 1 intermediate chain 1 |
DNCI1, DNCIC1 |
|
|
163
|
|
|
Dynein cytoplasmic 1 intermediate chain 2 |
DIC74, DNCI2, IC2, NEDMIBA |
|
|
164
|
|
|
Dynamin 2 |
CMT2M, CMTDI1, CMTDIB, DI-CMTB, DYN2, DYNII, LCCS5 |
Centronuclear myopathy, Centronuclear myopathy, x-linked, Charcot-marie-tooth disease, Congenital contracture, Congenital myopathy with fiber type disproportion, Congenital structural myopathy, Coronary heart disease, Cryptorchidism, Developmental delay, Distal amyotrophy, External ophthalmoplegia, Facial paralysis, Fetal akinesia-cerebral and retinal hemorrhage syndrome, Hemangioma, cavernous, Lethal congenital contracture syndrome, Lymphoblastic leukemia, Motor delay, Myopathy, Peripheral axonal neuropathy, Postnatal asphyxia, Prostate cancer, Ptosis, Sensorimotor neuropathy, Tubular aggregate myopathyView all (9 more) |
|
165
|
|
|
DNA methyltransferase 1 |
ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT, m.HsaI |
Adenocarcinoma, Anaplastic carcinoma, Anxiety disorder, Asthma, Bipolar disorder, Brainstem atrophy, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Cardiovascular diseases, Cataplexy, Cataract, Cerebellar ataxia, deafness and narcolepsy, Cerebellar atrophy, Cerebral atrophy, Colonic neoplasms, Deafness, Delirium, Dementia, Gastric cancer, Hearing loss, Hereditary insensitivity to pain with anhidrosis, Hereditary sensory and autonomic neuropathy, Hereditary sensory neuropathy-deafness-dementia syndrome, Marfan syndrome, Medulloblastoma, Medullomyoblastoma, Meningioma, Mental depression, Mood disorder, Narcolepsy, Nystagmus, Optic atrophy, Osteomyelitis, Pancreatic ductal carcinoma, Prostatic neoplasms, Prostate cancer, Renal carcinoma, Schizophrenia, Senile paranoid dementia, Sensory neuropathy, Sensory neuropathy, hereditary, Stomach neoplasmsView all (29 more) |
|
166
|
|
|
DNA methyltransferase 3 alpha |
DNMT3A2, HESJAS, M.HsaIIIA, TBRS |
Acquired kyphoscoliosis, Angioimmunoblastic t-cell lymphoma, Ankylosing spondylitis, Anxiety disorder, Arnold-chiari malformation, Atrial septal defect, Autism spectrum disorder, Autism, Bipolar disorder, Blepharophimosis, Breast cancer, Mammary neoplasms, Breast carcinoma, Cholangitis, Congenital exomphalos, Congenital kyphoscoliosis, Congenital microcephaly, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Cryptorchidism, Developmental regression, Dwarfism, Dysmorphic features, Eczema, Encephalomalacia, Esotropia, Glioblastoma, Granulomatous slack skin, Hypoplasia of the optic nerve, Ileocolitis, Mental retardation, Leukemia, Lung neoplasms, Lung adenocarcinoma, Lung cancer, Lymphoma, Macrocephaly, Major affective disorder, Malocclusion, Marfan syndrome, Microcephaly, Microlissencephaly, Monocytic leukemia, Movement disorders, Multiple congenital anomalies, Myelodysplastic syndrome, Myeloid leukemia, Myelomonocytic leukemia, Neuroendocrine tumors, Obesity, Patent ductus arteriosus, Promyelocytic leukemia, Psoriasis, Renal carcinoma, Schizophrenia, Seckel syndrome, Sezary syndrome, T-cell lymphoma, Tatton brown rahman syndrome, Tricuspid valve insufficiency, Ulcerative colitisView all (47 more) |
|
167
|
|
|
DNA methyltransferase 3 beta |
FSHD4, ICF, ICF1, M.HsaIIIB |
Anaplastic carcinoma, Anemia, Antibody deficiency syndrome, Autism spectrum disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Bronchiectasis, Carcinoma, Communicating hydrocephalus, Congenital epicanthus, Congenital exomphalos, Developmental delay, Dwarfism, Facioscapulohumeral dystrophy, Facioscapulohumeral muscular dystrophy, Bronchitis, Gastric cancer, Immunodeficiency-centromeric instability-facial anomalies syndrome, Immunodeficiency, Immunologic deficiency syndromes, Inflammatory bowel disease, Lymphopenia, Macrocephaly, Macroglossia, Malabsorption syndrome, Marfan syndrome, Mental retardation, Micrognathism, Mood disorder, Non-obstructive azoospermia, Perlman syndrome, Prostatic neoplasms, Prostate cancer, Prostate cancer, hereditary, Schizophrenia, Sinusitis, Stomach neoplasmsView all (23 more) |
|
168
|
|
|
Dedicator of cytokinesis 1 |
DOCK180, ced5 |
|
|
169
|
|
|
Dedicator of cytokinesis 2 |
IMD40 |
|
|
170
|
|
|
Dedicator of cytokinesis 3 |
MOCA, NEDIDHA, PBP |
Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital epicanthus, Developmental delay, Diverticular diseases, Dysmorphic features, High palate, Leukemia, Malocclusion, Movement disorders, Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia, Syndromic mental retardation |
