Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "D"
311 to 320 of 596 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

311
Delta like canonical Notch ligand 3
SCDO1
Astrocytoma, Spondylocostal dysostosis, Congenital abnormalities, Congenital cartilage disorder, Congenital fusion of ribs, Congenital hemivertebra, Craniofacial abnormalities, Desbuquois syndrome, Dysphoric mood, Jarcho-levin syndrome, Osteochondrodysplasias, Scoliosis, Syndactyly

312
Delta like canonical Notch ligand 4
AOS6, delta4, hdelta2
Adams-oliver syndrome, Aplasia cutis congenita, Breast neoplasms, Desbuquois syndrome, Multiple sclerosis

313
Dihydrolipoamide S-succinyltransferase
DLTS, KGD2, PGL7, PPGL7
Alzheimer disease, Migraine, Non-small cell lung carcinoma, Pheochromocytoma/paraganglioma syndrome

314
Distal-less homeobox 1
-
Autism, Bipolar disorder, Craniofacial abnormalities, Non-organic psychosis, Psychotic disorders, Schizophrenia

315
Distal-less homeobox 2
TES-1, TES1
Autism, Craniofacial abnormalities, Schizophrenia

316
Distal-less homeobox 3
AI4, TDO
Amelogenesis imperfecta, Dentin dysplasia, Dentinogenesis imperfecta, Desbuquois syndrome, Peripheral pulmonary artery stenosis, Tricho-dento-osseous syndrome

317
Distal-less homeobox 4
BP1, DLX7, DLX8, DLX9, OFC15
Cleft lip and palate, Orofacial cleft

318
Distal-less homeobox 5
SHFM1, SHFM1D
Alzheimer disease, Bone disease, Congenital cleft hand, Congenital malformation syndromes predominantly involving limbs, Craniofacial abnormalities, Desbuquois syndrome, Ectrodactyly, Gastroesophageal reflux disease, Klippel-trenaunay syndrome, Osteoarthritis, Rubinstein-taybi syndrome, Split hand-foot malformation, Thrombocytopenia, Vacterl association

319
Distal-less homeobox 6
-
Attention deficit hyperactivity disorder, Autism, Craniofacial abnormalities, Desbuquois syndrome, Ectrodactyly, Split hand-foot malformation, Substance abuse

320
Distal membrane arm assembly component 1
C9orf123, TMEM261
Attention deficit hyperactivity disorder, Cannabis abuse, Conduct disorder, Connective tissue disease, Conotruncal cardiac defect, Corneal astigmatism, Dementia, Dental caries, Insomnia, Osteonecrosis, Prostate cancer, Sarcopenia, Diabetes mellitus type 2