631
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|
|
DIS3 like 3'-5' exoribonuclease 2 |
FAM6A, PRLMNS, hDIS3L2 |
Curated: Androgenetic alopecia, Diabetic neuropathy, Neurodevelopmental disorder, Osteoarthritis, Perlman syndrome
Unreviewed: Agenesis Of Corpus Callosum, Anaplastic thyroid cancer, Aniridia, Cardiovascular Abnormalities, Colorectal Cancer, Colorectal neoplasm, Congenital Chromosomal Disease, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital Hypoplasia Of Penis, Cryptorchidism, Cutis marmorata telangiectatica congenita, Developmental Delay, Dolichocephaly, Dwarfism, Growth disorder, Hepatocellular carcinoma, Hernia, Femoral, Hyperinsulinism, Hypertension, Interrupted aortic arch, Intestinal Volvulus, Liver Cancer, Liver carcinoma, Liver neoplasms, Lung Neoplasms, Macrocephaly, Malignant Neoplasm, Mental retardation, Micrognathism, Neoplasms, Nephroblastoma, Posteriorly Rotated Ear, Ptosis, Specific Learning Disorder, Status Epilepticus, Strawberry Nevus Of Skin, Wilms tumor
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632
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|
|
DIS3 like 3'-5' exoribonuclease 2 pseudogene 1 |
DIS3L2P, FAM6B |
Curated: N/A
Unreviewed: N/A
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633
|
|
|
DISC1 scaffold protein |
C1orf136, SCZD9 |
Curated: Alzheimer disease, Amyotrophic lateral sclerosis, Anhedonia, Anxiety disorder, Asperger syndrome, Autism, Bell's palsy, Bipolar disorder, Fatigue syndrome, Color vision deficiency, Colorectal cancer, Bipolar depression, Major depressive disorder, Developmental coordination disorder, Peritoneal disease, Hyperkinesia, Intellectual developmental disorder, Internet addiction disorder, Mood disorder, Motor skills disorder, Pelvic organ prolapse, Schizophrenia, Scoliosis, Depression
Unreviewed: Affective Psychosis, Agenesis Of Corpus Callosum, Anxiety Disorder, Asperger Syndrome, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Behavior Disorders, Behcet Syndrome, Bipolar Disorder, Borderline personality disorder, Bronchopulmonary Dysplasia, Catalepsy, Cerebellar Hypoplasia, Chondrosarcoma, Cognition disorder, Cognitive disorder, Colorectal neoplasm, Congenital Microcephaly, Cortical development malformation, Craniometaphyseal dysplasia, Developmental Delay, Developmental dyspraxia, Diabetes Mellitus, Ear Diseases, Epilepsy, Frontotemporal dementia, Gaucher disease, Graves disease, Hepatocellular carcinoma, Hereditary neuropathy with liability to pressure palsies, Huntington Disease, Hyperlipidemia, Impaired Cognition, Lateral Sclerosis, Lissencephaly, Lung carcinoma, Major Affective Disorder, Manic Disorder, Melancholia, Mental Depression, Mental Disorders, Mental retardation, Microcephaly-Polymicrogyria-Corpus Callosum Agenesis Syndrome, Mitochondrial disease, Mood Disorder, Motor Skills Disorders, MYD88 Deficiency, Myocardial Infarction, Nervous System Disorder, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Neurodevelopmental Disorders, Nonorganic Psychosis, Obsessive-Compulsive Disorder, Osteochondroma, Panic disorder, Periodontitis, Polymicrogyria, Promyelocytic Leukemia, Psychosis, Psychotic disorders, Schizoaffective Disorder, Social Anhedonia, Testicular regression syndrome
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634
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|
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DISC1 intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
|
635
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|
|
DISC1 fusion partner 1 |
Boymaw |
Curated: N/A
Unreviewed: Age-related macular degeneration, Mental Disorders
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636
|
|
|
Disrupted in schizophrenia 2 |
DISC1-AS1, DISC1OS, NCRNA00015 |
Curated: N/A
Unreviewed: Asperger Syndrome, Autism, Autism Spectrum Disorder, Bipolar Disorder, Delusions, Hallucinations, Major Affective Disorder, Major depressive disorder, Mental Depression, Mental Disorders, Mood Disorder, Psychosis, Schizophrenia
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637
|
|
|
Dispatched RND transporter family member 1 |
DISPA, HPE10 |
Curated: Colorectal cancer, Esophageal atresia, Gastrointestinal stromal tumor, Holoprosencephaly, Microform holoprosencephaly, Syntelencephaly, Myocardial infarction, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly
Unreviewed: Agenesis Of Corpus Callosum, Alobar Holoprosencephaly, Ambiguous Genitalia, Asthma, Bipolar disorder, Choanal Atresia, Congenital Coloboma Of Iris, Congenital diaphragmatic hernia, Congenital Hypoplasia Of Penis, Craniofacial abnormalities, Cyclocephaly, Developmental dysplasia of the hip, Duodenal Atresia, Dwarfism, Fused incisors, Hemangioma, Hypothyroidism, Lobar Holoprosencephaly, Lung carcinoma, Mental retardation, Microcephaly, Microform Holoprosencephaly, Midline Interhemispheric Variant Of Holoprosencephaly, Obsessive-Compulsive Disorder, Orofacial cleft, Panhypopituitarism, Polydactyly, Posterolateral diaphragmatic hernia, Pulmonary hypoplasia, Renal agenesis, Scoliosis, Semilobar Holoprosencephaly, Septopreoptic Holoprosencephaly, Strabismus, Tetralogy of Fallot, Trichohepatoenteric Syndrome
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638
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|
|
Dispatched RND transporter family member 2 |
C15orf36, DISPB, HsT16908, LINC00594 |
Curated: Digestive system disease, Diverticular disease
Unreviewed: Lung Diseases
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639
|
|
|
Dispatched RND transporter family member 3 |
PTCHD2 |
Curated: Attention deficit hyperactivity disorder, Glaucoma
Unreviewed: Pancreatic Cyst
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640
|
|
|
DIX domain containing 1 |
CCD1 |
Curated: Anxiety disorder, Autism, Bipolar disorder, Bipolar depression, Major depressive disorder, Obesity, Schizophrenia
Unreviewed: Anxiety Disorder, Bipolar Disorder, Brain neoplasms, Breast Carcinoma, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Glioma, Hepatocellular carcinoma, Hodgkin Disease, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lymphoma, Malignant Neoplasm, Manic Disorder, Melancholia, Mental Depression, Neoplasms, Non-Hodgkin lymphoma, Prostate cancer, Retinoblastoma, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms
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