|
91
|
|
|
DENN domain containing 1B |
C1ORF18, C1orf218, FAM31B |
Ankylosing spondylitis, Anxiety disorder, Asthma, Biliary cirrhosis, Cholangitis, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Ileocolitis, Inflammatory bowel disease, Mental depression, Psoriasis, Biliary cholangitis, Ulcerative colitis |
|
92
|
|
|
Down syndrome chromosome region |
DSCR |
|
|
93
|
|
|
Dynactin subunit 1 |
DAP-150, DP-150, HMND14, P135 |
Amyotrophic lateral sclerosis, Anxiety disorder, Dementia, Distal amyotrophy, Distal hereditary motor neuronopathy, Dysarthria, Dyssomnia, Facial paralysis, Frontotemporal dementia, Laryngospasm, Lateral sclerosis, Mental depression, Mood disorder, Mood swings, Neuronopathy, Parkinson disease, Parkinsonian disease, Perry syndrome, Pseudobulbar palsy, Ramsay hunt paralysis syndrome, Respiratory failure, Sleep apnea, Sleep disorders, Supranuclear gaze palsy, Vocal cord paralysisView all (10 more) |
|
94
|
|
|
Doublecortin |
DBCN, DC, LISX, SCLH, XLIS |
Agenesis of corpus callosum, Agyria, Dysarthria, Fucosidase deficiency disease, Mental retardation, Lissencephaly, Lissencephaly, x-linked, Classical lissencephalies and subcortical band heterotopias, Malformation of cortical development, Miller dieker syndrome, Motor delay, Neuronal heterotopia, Nystagmus, Pachygyria, Penis agenesis, Subcortical band heterotopiaView all (1 more) |
|
95
|
|
|
Damage specific DNA binding protein 1 |
DDBA, UV-DDB1, WHIKERS, XAP1, XPCE, XPE, XPE-BF |
|
|
96
|
|
|
Damage specific DNA binding protein 2 |
DDBB, UV-DDB2, XPE |
Alopecia, Carcinoma, Cataract, Cerebral cortical atrophy, Congenital ankyloblepharon, Conjunctival telangiectasis, Conjunctivitis, Cryptorchidism, Developmental regression, Dwarfism, Ectropion, Entropion, Eye neoplasms, Hearing loss, Hyperkeratosis, Hypogonadism, Impaired cognition, Keratitis, Melanocytic nevus, Melanoma, Mental depression, Microcephaly, Mood disorder, Nervous system diseases, Optic atrophy, Papilloma, Poikiloderma, Pterygium, Skin carcinoma, Strabismus, Xeroderma pigmentosumView all (16 more) |
|
97
|
|
|
Dopa decarboxylase |
AADC |
Aromatic amino acid decarboxylase deficiency, Behavior disorders, Bipolar disorder, Choreoathetosis, Deficiency of aromatic-l-amino-acid decarboxylase, Developmental delay, Dysarthria, Dyssomnia, Extra-adrenal pheochromocytoma, Gastroesophageal reflux disease, Lymphoblastic leukemia, Major affective disorder, Mental disorders, Mental depression, Mental retardation, Miosis disorder, Mood swings, Parkinson disease, Parkinsonian disease, Pheochromocytoma, Ptosis, Ramsay hunt paralysis syndrome, Sleep disordersView all (8 more) |
|
98
|
|
|
Dynein assembly factor with WD repeats 1 |
CILD52, DNAAF18, ODA16, WDR69 |
|
|
99
|
|
|
DNA damage inducible transcript 3 |
AltDDIT3, C/EBPzeta, CEBPZ, CHOP, CHOP-10, CHOP10, GADD153 |
Arthritis, Asbestosis, Autoimmune diabetes, Breast cancer, Mammary neoplasms, Breast carcinoma, Colorectal cancer, Dermatitis, Diabetes mellitus, Brittle diabetes mellitus, Fatty liver, Glaucoma, Intestinal diseases, Juvenile arthritis, Liposarcoma, Marfan syndrome, Myocardial infarction, Myxoid liposarcoma, Nephrosis, Obesity, Ocular hypertension, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still diseaseView all (9 more) |
|
100
|
|
|
Dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit |
AGER1, CDG1R, GATD6, OKSWcl45, OST, OST48, WBP1 |
Blood coagulation disorders, Congenital disorder of glycosylation, Developmental delay, Dwarfism, Esotropia, Fatty liver, Gastroesophageal reflux disease, Lipodystrophy, Oromotor apraxia, Osteopenia, Hypothyroidism, Speech disorders, Strabismus |
