Health Conditions (D) - Genetics Home Reference (D)

Health Conditions - Genetics Home Reference

Health Conditions

Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.

1. Z

• D-bifunctional protein deficiency
• D-glycerate dehydrogenase deficiency, see Primary hyperoxaluria
• DA1, see Distal arthrogryposis type 1
• DA2A, see Freeman-Sheldon syndrome
• DA2B, see Sheldon-Hall syndrome
• DA9, see Congenital contractural arachnodactyly
• dacryosialoadenopathia atrophicans, see Sjögren syndrome
• DACS, see Congenital stromal corneal dystrophy
• DADA2, see Adenosine deaminase 2 deficiency
• dairy product intolerance, see Lactose intolerance
• Dandy-Walker complex, see Dandy-Walker malformation
• Dandy-Walker cyst, see Dandy-Walker malformation
• Dandy-Walker deformity, see Dandy-Walker malformation
• Dandy-Walker malformation
• Dandy-Walker syndrome, see Dandy-Walker malformation
• Danon disease
• Dappled metaphysis syndrome, see Spondyloepimetaphyseal dysplasia, Strudwick type
• Darier disease
• Darier's Disease, see Darier disease
• Darier-Ferrand tumor, see Dermatofibrosarcoma protuberans
• Darier-Hoffmann tumor, see Dermatofibrosarcoma protuberans
• Darier-White disease, see Darier disease
• dark dot disease, see Dowling-Degos disease
• DAT, see Alzheimer disease
• Davidson disease, see Microvillus inclusion disease
• DBA, see Diamond-Blackfan anemia
• DBMD, see Duchenne and Becker muscular dystrophy
• DBP deficiency, see D-bifunctional protein deficiency
• DBS, see Donnai-Barrow syndrome
• DBS/FOAR syndrome, see Donnai-Barrow syndrome
• DCMA, see Dilated cardiomyopathy with ataxia syndrome
• DCMA syndrome, see Dilated cardiomyopathy with ataxia syndrome
• DCO, see Léri-Weill dyschondrosteosis
• DDC deficiency, see Aromatic l-amino acid decarboxylase deficiency
• DDD, see Dowling-Degos disease
• DDD, see C3 glomerulopathy
• DDD/MPGNII, see C3 glomerulopathy
• DDPAC, see Frontotemporal dementia with parkinsonism-17
• DDS, see Denys-Drash syndrome
• DDU, see Vibratory urticaria
• De Grouchy syndrome, see Distal 18q deletion syndrome
• De la Chapelle dysplasia, see Atelosteogenesis type 2
• de Lange syndrome, see Cornelia de Lange syndrome
• De Morsier syndrome, see Septo-optic dysplasia
• de Toni-Caffey disease, see Caffey disease
• De Vivo disease, see GLUT1 deficiency syndrome
• deafness and myopia, see Deafness and myopia syndrome
• Deafness and myopia syndrome
• deafness and pili torti, Bjornstad type, see Björnstad syndrome
• deafness due to old age, see Age-related hearing loss
• deafness with goiter, see Pendred syndrome
• deafness with LAMM, see Congenital deafness with labyrinthine aplasia, microtia, and microdontia
• deafness, cochlear, plus, see Deafness and myopia syndrome
• deafness, congenital, and functional heart disease, see Jervell and Lange-Nielsen syndrome
• deafness, onychodystrophy, osteodystrophy, and mental retardation syndrome, see DOORS syndrome
• Deafness-dystonia syndrome, see Deafness-dystonia-optic neuronopathy syndrome
• Deafness-dystonia-optic neuronopathy syndrome
• deafness-imperforate anus-hypoplastic thumbs syndrome, see Townes-Brocks Syndrome
• deafness-infertility syndrome, see Sensorineural deafness and male infertility
• deafness-oncychodystrophy-osteodystrophy-intellectual disability syndrome, see DOORS syndrome
• deafness-onychoosteodystrophy-intellectual disability syndrome, see DOORS syndrome
• deafness-retinitis pigmentosa syndrome, see Usher syndrome
• debrancher deficiency, see Glycogen storage disease type III
• decorin-associated congenital stromal corneal dystrophy, see Congenital stromal corneal dystrophy
• deep fibromatosis, see Desmoid tumor
• defect of enterocyte intrinsic factor receptor, see Imerslund-Gräsbeck syndrome
• defective color vision, see Color vision deficiency
• deficiency disease, phenylalanine hydroxylase, see Phenylketonuria
• deficiency mutase phosphoglycerate, see Phosphoglycerate mutase deficiency
• deficiency of 3-hydroxyacyl-CoA dehydrogenase, see 3-hydroxyacyl-CoA dehydrogenase deficiency
• deficiency of 3beta-hydroxysterol delta24-reductase, see Desmosterolosis
• deficiency of acyl-CoA dehydrogenase family member 9, see ACAD9 deficiency
• deficiency of ADA2, see Adenosine deaminase 2 deficiency
• Deficiency of alkaline phosphatase, see Hypophosphatasia
• deficiency of alpha-glucosidase, see Pompe disease
• deficiency of alpha-mannosidase, see Alpha-mannosidosis
• deficiency of aromatic-L-amino-acid decarboxylase, see Aromatic l-amino acid decarboxylase deficiency
• deficiency of beta-ureidopropionase, see Beta-ureidopropionase deficiency
• deficiency of butyryl-CoA dehydrogenase, see Short-chain acyl-CoA dehydrogenase deficiency
• deficiency of butyrylcholine esterase, see Pseudocholinesterase deficiency
• deficiency of cathepsin A, see Galactosialidosis
• deficiency of cytochrome-b5 reductase, see Autosomal recessive congenital methemoglobinemia
• deficiency of factor XIII, see Factor XIII deficiency
• deficiency of ferroxidase, see Aceruloplasminemia
• deficiency of glucose-6-phosphate dehydrogenase, see Glucose-6-phosphate dehydrogenase deficiency
• deficiency of glutathione synthase, see Glutathione synthetase deficiency
• deficiency of glutathione synthetase, see Glutathione synthetase deficiency
• deficiency of glycoprotein complex IIb-IIIa, see Glanzmann thrombasthenia
• deficiency of guanidinoacetate methyltransferase, see Guanidinoacetate methyltransferase deficiency
• deficiency of guanine phosphoribosyltransferase, see Lesch-Nyhan syndrome
• Deficiency of hydroxymethylglutaryl-CoA lyase, see 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
• deficiency of hypoxanthine phosphoribosyltransferase, see Lesch-Nyhan syndrome
• deficiency of isobutyryl-CoA dehydrogenase, see Isobutyryl-CoA dehydrogenase deficiency
• deficiency of lactate dehydrogenase, see Lactate dehydrogenase deficiency
• deficiency of luteinizing hormone-releasing hormone with ataxia, see Gordon Holmes syndrome
• deficiency of malonyl-CoA decarboxylase, see Malonyl-CoA decarboxylase deficiency
• Deficiency of methionine adenosyltransferase, see Hypermethioninemia
• Deficiency of methylcrotonoyl-CoA carboxylase, see 3-methylcrotonyl-CoA carboxylase deficiency
• deficiency of molybdenum cofactor, see Molybdenum cofactor deficiency
• deficiency of monoamine oxidase A, see Monoamine oxidase A deficiency
• deficiency of N-glycanase 1, see NGLY1-congenital disorder of deglycosylation
• deficiency of phosphotriose isomerase, see Triosephosphate isomerase deficiency
• deficiency of platelet fibrinogen receptor, see Glanzmann thrombasthenia
• deficiency of platelet glycoprotein 1b, see Bernard-Soulier syndrome
• deficiency of steroid 11-beta-monooxygenase, see Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
• deficiency of steroid 17-alpha-monooxygenase, see 17 alpha-hydroxylase/17,20-lyase deficiency
• deficiency of the aminoacylase-1 enzyme, see Aminoacylase 1 deficiency
• deficiency of the interleukin-36 receptor antagonist, see Generalized pustular psoriasis
• deficiency, Laki-Lorand factor, see Factor XIII deficiency
• deficient alpha granule syndrome, see Gray platelet syndrome
• degenerative joint disease, see Osteoarthritis
• degenerative polyarthritis, see Osteoarthritis
• degenerative retinoschisis, see X-linked juvenile retinoschisis
• del(18q) syndrome, see Distal 18q deletion syndrome
• del(18q) syndrome, see Proximal 18q deletion syndrome
• del(3p) syndrome, see 3p deletion syndrome
• del(4p) syndrome, see Wolf-Hirschhorn syndrome
• deletion 17p syndrome, see Smith-Magenis syndrome
• deletion 17q12, see 17q12 deletion syndrome
• deletion 22q11.2 syndrome, see 22q11.2 deletion syndrome
• deletion 22q13 syndrome, see 22q13.3 deletion syndrome
• deletion 22q13.3 syndrome, see 22q13.3 deletion syndrome
• deletion 3p, see 3p deletion syndrome
• dementia of the Lewy body type, see Dementia with Lewy bodies
• dementia praecox, see Schizophrenia
• dementia with amyotrophic lateral sclerosis, see Amyotrophic lateral sclerosis
• Dementia with Lewy bodies
• dementia, Lewy body, see Dementia with Lewy bodies
• demyelinogenic leukodystrophy, see Alexander disease
• dense deposit disease, see C3 glomerulopathy
• Dent disease
• Dent's disease, see Dent disease
• Dentatorubral-pallidoluysian atrophy
• Dentinogenesis imperfecta
• dento-osseous dysplasia, see Cleidocranial dysplasia
• dentoleukoencephalopathy, see Pol III-related leukodystrophy
• Dents disease, see Dent disease
• Denys-Drash syndrome
• Deoxyguanosine kinase deficiency
• Depression
• depression in a seasonal pattern, see Seasonal affective disorder
• depression, bipolar, see Bipolar disorder
• depression; seasonal, see Seasonal affective disorder
• depressive disorder, see Depression
• Der(22) syndrome due to 3:1 meiotic disjunction events, see Emanuel syndrome
• Dercum disease, see Adiposis dolorosa
• Dercum's disease, see Adiposis dolorosa
• Dercum-Vitaut syndrome, see Adiposis dolorosa
• dermal eccrine cylindroma, see Familial cylindromatosis
• dermatofibrosarcoma, see Dermatofibrosarcoma protuberans
• Dermatofibrosarcoma protuberans
• dermatofibrosis disseminata lenticularis, see Buschke-Ollendorff syndrome
• dermatofibrosis lenticularis disseminata, see Buschke-Ollendorff syndrome
• dermatofibrosis lenticularis disseminata with osteopoikilosis, see Buschke-Ollendorff syndrome
• dermatofibrosis, disseminated, with osteopoikilosis, see Buschke-Ollendorff syndrome
• dermatolysis, see Cutis laxa
• dermatomegaly, see Cutis laxa
• dermatoosteopoikilosis, see Buschke-Ollendorff syndrome
• dermodistortive urticaria, see Vibratory urticaria
• DES-VLDLR, see VLDLR-associated cerebellar hypoplasia
• DeSanctis-Cacchione syndrome, see Xeroderma pigmentosum
• desmoid fibromatosis, see Desmoid tumor
• Desmoid tumor
• Desmosterolosis
• developmental verbal dyspraxia, see FOXP2-related speech and language disorder
• Devic disease, see Neuromyelitis optica
• Devic neuromyelitis optica, see Neuromyelitis optica
• Devic syndrome, see Neuromyelitis optica
• Devic's disease, see Neuromyelitis optica
• DFNMYP, see Deafness and myopia syndrome
• DFSP, see Dermatofibrosarcoma protuberans
• DGI, see Dentinogenesis imperfecta
• DGSX, see Simpson-Golabi-Behmel syndrome
• DGUOK-related mitochondrial DNA depletion syndrome, see Deoxyguanosine kinase deficiency
• DHA crystalline nephropathy, see Adenine phosphoribosyltransferase deficiency
• DHMN-V, see Distal hereditary motor neuropathy, type V
• DHMN6, see Spinal muscular atrophy with respiratory distress type 1
• DHTR deficiency, see Androgen insensitivity syndrome
• diabetes insipidus and mellitus with optic atrophy and deafness, see Wolfram syndrome
• diabetes insipidus renalis, see Nephrogenic diabetes insipidus
• diabetes insipidus secondary to vasopressin deficiency, see Neurohypophyseal diabetes insipidus
• diabetes insipidus, central, see Neurohypophyseal diabetes insipidus
• diabetes insipidus, diabetes mellitus, optic atrophy, and deafness, see Wolfram syndrome
• diabetes insipidus, nephrogenic, see Nephrogenic diabetes insipidus
• diabetes insipidus, neurogenic, see Neurohypophyseal diabetes insipidus
• diabetes insipidus, neurohypophyseal, see Neurohypophyseal diabetes insipidus
• diabetes insipidus, pituitary, see Neurohypophyseal diabetes insipidus
• diabetes mellitus arising in pregnancy, see Gestational diabetes
• diabetes mellitus type 1, see Type 1 diabetes
• diabetes mellitus, adult-onset, see Type 2 diabetes
• diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea, see Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
• diabetes mellitus, gestational, see Gestational diabetes
• diabetes mellitus, insulin-dependent, see Type 1 diabetes
• diabetes mellitus, insulin-resistant, with acanthosis nigricans, see Type A insulin resistance syndrome
• diabetes mellitus, non-insulin-dependent, see Type 2 diabetes
• diabetes mellitus, pregnancy related, see Gestational diabetes
• diabetes mellitus, type 1, see Type 1 diabetes
• diabetes mellitus, type 2, see Type 2 diabetes
• diabetes mellitus, type II, see Type 2 diabetes
• diabetes mellitus, type II, with deafness, see Maternally inherited diabetes and deafness
• diabetes, pregnancy-induced, see Gestational diabetes
• diabetes-hypogonadism-deafness-intellectual disability syndrome, see Woodhouse-Sakati syndrome
• Diamond-Blackfan anemia
• diaphorase deficiency, see Autosomal recessive congenital methemoglobinemia
• diaphragmatic hernia, abnormal face, and distal limb anomalies, see Fryns syndrome
• diaphragmatic hernia-exomphalos-corpus callosum agenesis, see Donnai-Barrow syndrome
• Diaphragmatic hernia-exomphalos-hypertelorism syndrome, see Donnai-Barrow syndrome
• diaphragmatic spinal muscular atrophy, see Spinal muscular atrophy with respiratory distress type 1
• diaphyseal aclasis, see Hereditary multiple osteochondromas
• diaphyseal dysplasia, see Camurati-Engelmann disease
• diaphyseal dysplasia associated with anemia, see Ghosal hematodiaphyseal dysplasia
• diaphyseal hyperostosis, see Camurati-Engelmann disease
• diaphyseal osteosclerosis, see Camurati-Engelmann disease
• diarrhea, fatal infantile, with trichorrhexis nodosa, see Trichohepatoenteric syndrome
• diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked, see Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
• diarrhea, syndromic, see Trichohepatoenteric syndrome
• Diastrophic dwarfism, see Diastrophic dysplasia
• Diastrophic dysplasia
• DICER1 syndrome
• DICER1-related pleuropulmonary blastoma cancer predisposition syndrome, see DICER1 syndrome
• DIDMOAD, see Wolfram syndrome
• DIDMOAD syndrome, see Wolfram syndrome
• DIDMOADUD, see Wolfram syndrome
• diffuse arterial calcifying elastopathy of infancy, see Generalized arterial calcification of infancy
• diffuse cerebral sclerosis of Schilder, see Alpers-Huttenlocher syndrome
• diffuse globoid body sclerosis, see Krabbe disease
• diffuse lentiginosis, see Noonan syndrome with multiple lentigines
• diffuse Lewy body disease, see Dementia with Lewy bodies
• DiGeorge syndrome, see 22q11.2 deletion syndrome
• digitorenocerebral syndrome, see DOORS syndrome
• Dihydrolipoamide dehydrogenase deficiency
• dihydrolipoyl dehydrogenase deficiency, see Dihydrolipoamide dehydrogenase deficiency
• Dihydropyrimidinase deficiency
• Dihydropyrimidine dehydrogenase deficiency
• dihydropyrimidinuria, see Dihydropyrimidine dehydrogenase deficiency
• dihydropyrimidinuria, see Dihydropyrimidinase deficiency
• dihydrotestosterone receptor deficiency, see Androgen insensitivity syndrome
• dihydrouracil amidohydrolase deficiency, see Dihydropyrimidinase deficiency
• dilated cardiomyopathy 3B, see X-linked dilated cardiomyopathy
• Dilated cardiomyopathy with ataxia syndrome
• DIS, see Sensorineural deafness and male infertility
• disaccharide intolerance I, see Congenital sucrase-isomaltase deficiency
• discogenic disease, see Intervertebral disc disease
• discogenic disorder, see Intervertebral disc disease
• disinhibition-dementia-parkinsonism-amytrophy complex, see Frontotemporal dementia with parkinsonism-17
• disorder of intervertebral disc, see Intervertebral disc disease
• disseminated lupus erythematosus, see Systemic lupus erythematosus
• disseminated sclerosis, see Multiple sclerosis
• Distal 18q deletion syndrome
• Distal arthrogryposis type 1
• distal arthrogryposis type 2B, see Sheldon-Hall syndrome
• distal arthrogryposis, type 2A, see Freeman-Sheldon syndrome
• distal arthrogyropsis type 9, see Congenital contractural arachnodactyly
• distal hereditary motor neuronopathy type 5, see Distal hereditary motor neuropathy, type V
• distal hereditary motor neuronopathy type VI, see Spinal muscular atrophy with respiratory distress type 1
• distal hereditary motor neuronopathy, type II, see Distal hereditary motor neuropathy, type II
• distal hereditary motor neuronopathy, type V, see Distal hereditary motor neuropathy, type V
• Distal hereditary motor neuropathy, type II
• Distal hereditary motor neuropathy, type V
• distal monosomy 1p36, see 1p36 deletion syndrome
• distal muscular dystrophy, Miyoshi type, see Miyoshi myopathy
• distal myopathy 1, see Laing distal myopathy
• Distal myopathy 2
• Distal myopathy with rimmed vacuoles, see Inclusion body myopathy 2
• distal myopathy with vocal cord and pharyngeal signs, see Distal myopathy 2
• distal myopathy with vocal cord weakness, see Distal myopathy 2
• distal myopathy, Tateyama type, see CAV3-related distal myopathy
• distal spinal muscular atrophy type 1, see Spinal muscular atrophy with respiratory distress type 1
• distal spinal muscular atrophy, type V, see Distal hereditary motor neuropathy, type V
• distichiasis-lymphedema syndrome, see Lymphedema-distichiasis syndrome
• DITRA, see Generalized pustular psoriasis
• DJS, see Dubin-Johnson syndrome
• DK1 deficiency, see DOLK-congenital disorder of glycosylation
• DLB, see Dementia with Lewy bodies
• DLD deficiency, see Dihydrolipoamide dehydrogenase deficiency
• DMD-associated dilated cardiomyopathy, see X-linked dilated cardiomyopathy
• DMD-related dilated cardiomyopathy, see X-linked dilated cardiomyopathy
• DMRV, see Inclusion body myopathy 2
• DNAJC19 defect, see Dilated cardiomyopathy with ataxia syndrome
• DNAJC19 defect, see Barth syndrome
• DNMT1-complex disorder, see Hereditary sensory and autonomic neuropathy type IE
• DNMT1-related dementia, deafness, and sensory neuropathy, see Hereditary sensory and autonomic neuropathy type IE
• DNMT3A overgrowth syndrome
• DOA, see Optic atrophy type 1
• DOCK8 deficiency, see Autosomal recessive hyper-IgE syndrome
• DOCK8 immunodeficiency syndrome, see Autosomal recessive hyper-IgE syndrome
• dolichol kinase deficiency, see DOLK-congenital disorder of glycosylation
• dolichospondylic dysplasia, see 3-M syndrome
• DOLK-CDG, see DOLK-congenital disorder of glycosylation
• DOLK-congenital disorder of glycosylation
• dominant optic atrophy, see Optic atrophy type 1
• Donnai-Barrow syndrome
• Donohue syndrome
• Donohue's syndrome, see Donohue syndrome
• DOOR syndrome, see DOORS syndrome
• DOORS syndrome
• dopa decarboxylase deficiency, see Aromatic l-amino acid decarboxylase deficiency
• Dopa-responsive dystonia
• dopa-responsive dystonia due to sepiapterin reductase deficiency, see Sepiapterin reductase deficiency
• Dopamine beta-hydroxylase deficiency
• Dopamine transporter deficiency syndrome
• dopamine β-hydroxylase, see Dopamine beta-hydroxylase deficiency
• Dowling-Degos disease
• Dowling-Degos-Kitamura disease, see Dowling-Degos disease
• Down syndrome
• Down's syndrome, see Down syndrome
• DPD deficiency, see Dihydropyrimidine dehydrogenase deficiency
• DPH deficiency, see Dihydropyrimidinase deficiency
• DPR, see Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis
• DPYS deficiency, see Dihydropyrimidinase deficiency
• Drash syndrome, see Denys-Drash syndrome
• DRC syndrome, see DOORS syndrome
• DRD, see Dopa-responsive dystonia
• DRPLA, see Dentatorubral-pallidoluysian atrophy
• DRRS, see Duane-radial ray syndrome
• drug-induced Stevens Johnson syndrome, see Stevens-Johnson syndrome/toxic epidermal necrolysis
• DSMA1, see Spinal muscular atrophy with respiratory distress type 1
• DSMAV, see Distal hereditary motor neuropathy, type V
• DTD, see Diastrophic dysplasia
• DTDS, see Dopamine transporter deficiency syndrome
• DTM1, see CHMP2B-related frontotemporal dementia
• Duane anomaly, isolated, see Isolated Duane retraction syndrome
• Duane retraction syndrome, see Isolated Duane retraction syndrome
• Duane syndrome, see Isolated Duane retraction syndrome
• Duane's syndrome, see Isolated Duane retraction syndrome
• Duane-radial ray syndrome
• Dubin-Johnson syndrome
• Duchenne and Becker muscular dystrophy
• Duchenne/Becker muscular dystrophy, see Duchenne and Becker muscular dystrophy
• Duncan disease, see X-linked lymphoproliferative disease
• Dunnigan-Kobberling syndrome, see Familial partial lipodystrophy
• dup(17)(p11.2p11.2), see Potocki-Lupski syndrome
• dup(7)(q11.23), see 7q11.23 duplication syndrome
• duplication 17p11.2 syndrome, see Potocki-Lupski syndrome
• duplication/inversion 15q11, see Isodicentric chromosome 15 syndrome
• Dupuytren contracture
• Dupuytren's contracture, see Dupuytren contracture
• Dupuytren's disease, see Dupuytren contracture
• dwarf, achondroplastic, see Achondroplasia
• Dwarf, thanatophoric, see Thanatophoric dysplasia
• dwarfism, growth hormone deficiency, see Isolated growth hormone deficiency
• dwarfism, pituitary, see Isolated growth hormone deficiency
• dwarfism-onychodysplasia, see Coffin-Siris syndrome
• dwarfism-retinal atrophy-deafness syndrome, see Cockayne syndrome
• DWM, see Dandy-Walker malformation
• DWS, see Dandy-Walker malformation
• dyschondroplasia, see Ollier disease
• dyschondroplasia and cavernous hemangioma, see Maffucci syndrome
• dyschondrosteosis, see Léri-Weill dyschondrosteosis
• dyschondrosteosis homozygous, see Langer mesomelic dysplasia
• dysencephalia splanchnocystica, see Meckel syndrome
• dysequilibrium syndrome-VLDLR, see VLDLR-associated cerebellar hypoplasia
• Dyserythropoietic anemia and thrombocytopenia
• dyserythropoietic anemia with thrombocytopenia, see Dyserythropoietic anemia and thrombocytopenia
• dysgenesis neuroepithelialis retinae, see Leber congenital amaurosis
• dysgnathia complex, see Auriculo-condylar syndrome
• Dyskeratosis congenita
• dyslipoproteinemic corneal dystrophy, see Fish-eye disease
• dysmyelinating leukodystrophy and spastic paraparesis, see Fatty acid hydroxylase-associated neurodegeneration
• dysmyelinogenic leukodystrophy, see Alexander disease
• dysostosis craniofacialis with hypertelorism, see Saethre-Chotzen syndrome
• dysplasia linguofacialis, see Oral-facial-digital syndrome
• dysprothrombinemia, see Prothrombin deficiency
• dystonia 10, see Familial paroxysmal kinesigenic dyskinesia
• dystonia 11, see Myoclonus-dystonia
• Dystonia 3, torsion, X-linked, see X-linked dystonia-parkinsonism
• dystonia 5, dopa-responsive type, see Dopa-responsive dystonia
• Dystonia 6
• dystonia musculorum deformans, see X-linked dystonia-parkinsonism
• Dystonia musculorum deformans 1, see Early-onset primary dystonia
• Dystonia-parkinsonism, X-linked, see X-linked dystonia-parkinsonism
• dystrophia brevicollis congenita, see Klippel-Feil syndrome
• dystrophia corneae parenchymatosa congenita, see Congenital stromal corneal dystrophy
• dystrophia myotonica, see Myotonic dystrophy
• Dystrophic epidermolysis bullosa
• dystrophy, oculopharyngeal muscular, see Oculopharyngeal muscular dystrophy
• DYT1, see Early-onset primary dystonia
• DYT11, see Myoclonus-dystonia
• DYT12, see Rapid-onset dystonia parkinsonism
• DYT3, see X-linked dystonia-parkinsonism
• DYT6, see Dystonia 6
• DYT6 dystonia, see Dystonia 6