731
|
|
|
DMTF1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
732
|
|
|
Dematin actin binding protein |
DMT, EPB49 |
Curated: N/A
Unreviewed: Anemia, Anxiety Disorder, Colorectal Cancer, Fuchs Endothelial Dystrophy, Hemolytic anemia, Hereditary Spherocytosis, Impaired Cognition, Malignant Neoplasm, Mental Depression, Mitral Valve Stenosis, Mixed Anxiety And Depressive Disorder, Mood Disorder, Multiple Sclerosis, Prostate adenocarcinoma, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Spherocytosis, Stomach neoplasms, Vascular ring
|
733
|
|
|
DM1 locus, WD repeat containing |
D19S593E, DMR-N9, DMRN9, gene59 |
Curated: Obstructive pulmonary disease, Respiratory system disease
Unreviewed: Chronic Obstructive Pulmonary Disease, Myotonic dystrophy, Oligospermia
|
734
|
|
|
Dmx like 1 |
- |
Curated: Alzheimer disease, Coronary artery disease, Glioma, Myocardial infarction
Unreviewed: Astrocytoma, Glaucoma, Glioblastoma, Open angle glaucoma
|
735
|
|
|
DMXL1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
736
|
|
|
Dmx like 2 |
DEE81, DFNA71, EIEE81, PEPNS, RC3 |
Curated: Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Developmental and epileptic encephalopathy, Hearing loss, Insomnia, Major depressive disorder, Metabolic syndrome, Pituitary stalk interruption syndrome, Primary aldosteronism, Diabetes mellitus type 2, nonsyndromic genetic hearing loss
Unreviewed: Autism spectrum disorder, Behcet disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Central hypothyroidism, Cerebellar vermis agenesis, Developmental disability, Dwarfism, Dysarthria, Epileptic Encephalopathy, Hearing Loss, Hypoglycemia, Hypogonadism, Hypogonadotropic hypogonadism, Lung neoplasms, Mental retardation, Motor delay, Neurodevelopmental Disorders, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Polyendocrine-Polyneuropathy Syndrome, Polyneuropathy, Psoriasis, Spasms X-Linked, Stroke
|
737
|
|
|
DNA replication helicase/nuclease 2 |
DNA2L, RTS4, hDNA2 |
Curated: Congenital myopathy, Desbuquois syndrome, Dna2-related mitochondrial dna deletion syndrome, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Mitochondrial myopathy, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Rothmund-thomson syndrome, Seckel syndrome, Sheehan syndrome, mitochondrial disease
Unreviewed: Acquired Kyphoscoliosis, Alternating hemiplegia of childhood, Amyotrophy, Anemia, Bladder carcinoma, Bladder Neoplasm, Bloom Syndrome, Breast Cancer, Breast Carcinoma, Breast neoplasm, Colorectal neoplasm, Congenital kyphoscoliosis, Congenital ptosis, Developmental Delay, Dwarfism, Ectopic kidney, Endometrial neoplasm, Endometriosis, External Ophthalmoplegia, Facial paralysis, Fanconi Anemia, Leukemia, Li-Fraumeni Syndrome, Lynch syndrome, Malignant Neoplasm, Mental Depression, Mental retardation, Microcephaly, Micrognathism, Mitochondrial DNA Deletion Syndrome, Multiple system atrophy, Myeloproliferative disorder, Myopathy, Neoplasms, Ophthalmoplegia, Ovarian cancer, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Progressive External Ophthalmoplegia, Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Ptosis, Seckel Syndrome, Sleep Apnea, Spinal cord compression, Urinary bladder cancer, Visceral neuropathy, Werner Syndrome
|
738
|
|
|
Dynein axonemal assembly factor 1 |
CILD13, DAU1, LRRC50, ODA7, swt |
Curated: Autism, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Situs ambiguus, primary ciliary dyskinesia 13
Unreviewed: Asplenia, Asthenozoospermia, Asthma, Bronchiectasis, Bronchitis, Ciliopathies, Congenital abnormalities, Congenital Pectus Excavatum, Congestive Heart Failure, Corneal Dystrophy, Coronary Heart Disease, Cystic Kidney Disease, Gastric Cancer, Hearing Loss, Heart Failure, Hydrocephalus, Hypertension, Infertility, Kartagener Syndrome, Lateral Sclerosis, Lung Diseases, Nasal polyposis, Nasopharyngeal carcinoma, Neoplasms, Neural tube defect, Otitis media, Polycystic kidney disease, Rhinitis, Scoliosis, Seminoma, Sinusitis, Situs Inversus, Testicular Germ Cell Tumor
|
739
|
|
|
Dynein axonemal assembly factor 10 |
WDR92 |
Curated: Lung cancer, Osteoarthritis, Squamous cell carcinoma
Unreviewed: Breast Cancer, Breast Carcinoma, Carcinogenesis, Chronic disease, Coronary artery disease, Varicose veins
|
740
|
|
|
Dynein axonemal assembly factor 11 |
CILD19, LRRC6, LRTP, TSLRP, tilB |
Curated: Ciliary dyskinesia, Congenital nasopharyngeal atresia, Sarcoidosis, Scoliosis, Situs ambiguus, primary ciliary dyskinesia 19
Unreviewed: Asplenia, Asthenozoospermia, Asthma, Bronchiectasis, Congenital Pectus Excavatum, Corneal Dystrophy, Gastric Cancer, Hearing Loss, Hydrocephalus, Infertility, Kartagener Syndrome, Lung Diseases, Male infertility, Nasal polyposis, Otitis media, Rhinitis, Sinusitis, Situs Inversus
|