Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "D"

141 to 150 of 466 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
141	1747	DLX3	Distal-less homeobox 3	AI4, TDO	Amelogenesis imperfecta, Amelogenesis imperfecta with taurodontism, Clinodactyly, Dolichocephaly, Frontal bossing, Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism, Hypomineralization of enamel of tooth, Microdontia, Osteosclerosis, Peripheral pulmonary artery stenosis, Taurodontism, Trichodentoosseous syndrome
142	1748	DLX4	Distal-less homeobox 4	BP1, DLX7, DLX8, DLX9, OFC15	Congenital epicanthus, Congenital euryblepharon, Cryptorchidism, Hearing loss, Hypoplasia of the maxilla, Malnutrition, Oropharyngeal dysphagia, Orofacial cleft, Otitis media, Velopharyngeal insufficiency
143	1749	DLX5	Distal-less homeobox 5	SHFM1, SHFM1D	Alzheimer disease, Aniridia, Bone disease, Ectrodactyly, Hearing loss, Isolated split hand-split foot malformation, Oligodactyly, Split hand foot deformity, Split hand-split foot-deafness syndrome, Split-hand-foot malformation with sensorineural hearing loss, Syndactyly of fingers
144	1750	DLX6	Distal-less homeobox 6	-	Aniridia, Ectrodactyly, Hearing loss, Isolated split hand-split foot malformation, Oligodactyly, Split hand foot deformity, Split-hand-foot malformation with sensorineural hearing loss, Syndactyly of fingers
145	1755	DMBT1	Deleted in malignant brain tumors 1	GP340, SAG, SALSA, muclin	Colonic neoplasms, Glioma
146	1756	DMD	Dystrophin	BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85	Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Becker muscular dystrophy, Breast cancer, Bronchopulmonary dysplasia, Camptodactyly of fingers, Cardiomyopathy, Colorectal cancer, Congenital pectus excavatum, Congestive heart failure, Developmental delay, Dilated cardiomyopathy, Duchenne and becker muscular dystrophy, Duchenne muscular dystrophy View all (35 more)
147	1758	DMP1	Dentin matrix acidic phosphoprotein 1	ARHP, ARHR, DMP-1	Acromesomelic dysplasia, Brachydactyly, Chondrodysplasia punctata, Craniosynostosis, Dwarfism, Enthesitis, Fibular hypoplasia and complex brachydactyly, Hearing loss, Hypophosphatemic rickets, Hypophosphatemic vitamin d refractory rickets, x-linked, Malabsorption syndrome, Multiple synostoses syndrome, Osteoarthritis of hip, Osteochondrodysplasia, Osteosclerosis View all (6 more)
148	1759	DNM1	Dynamin 1	DEE31, DEE31A, DEE31B, DNM, EIEE31	Absence seizure, Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Dysmorphic features, Epilepsy, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Hypotonic seizures, Lennox-gastaut syndrome View all (14 more)
149	1760	DMPK	DM1 protein kinase	DM, DM1, DM1PK, DMK, MDPK, MT-PK	Atrioventricular block, Cataract, Cerebral atrophy, Cholelithiasis, Congenital myotonic dystrophy, Cryptorchidism, Dysphagia, Facial paralysis, Hernia of abdominal wall, Hydrocephalus, Hypogonadism, Mental retardation, Lung carcinoma, Myotonic dystrophy, Steinert myotonic dystrophy, Strabismus, Testicular atrophy View all (2 more)
150	1761	DMRT1	Doublesex and mab-3 related transcription factor 1	CT154, DMT1	46, xy complete gonadal dysgenesis, 46, xy sex reversal, Neoplasm, Embryonal neoplasm, Tumor, Gonadal dysgenesis, Hypogonadotropic hypogonadism, Male pseudohermaphroditism, Malignant neoplasm of testis, Malignant testicular germ cell tumor, Non-obstructive azoospermia, Polycystic ovary syndrome, Tumor of rete testis, Swyer syndrome, Testicular neoplasms View all (2 more)

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