List of diseases (D)
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Diseases |
D
Da
- Daentl Towsend Siegel syndrome
- Dahlberg Borer Newcomer syndrome
- Daish Hardman Lamont syndrome
- Dandy Walker facial hemangioma
- Dandy Walker malformation postaxial polydactyly
- Dandy Walker syndrome recessive form
- Dandy-walker malformation with mental retardation, basal ganglia disease, and seizures
- Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
- Dandy-Walker syndrome
- Daneman Davy Mancer syndrome
- Darier's disease
- Davenport Donlan syndrome
- David syndrome
- Davis Lafer syndrome
De
Dea
Deaf
Deafn
Deafne
Deafness c-Deafness s
- Deafness conductive ptosis skeletal anomalies
- Deafness conductive stapedial ear malformation facial palsy
- Deafness congenital onychodystrophy recessive
- Deafness craniofacial syndrome
- Deafness enamel hypoplasia nail defects
- Deafness epiphyseal dysplasia short stature
- Deafness goiter stippled epiphyses
- Deafness hyperuricemia neurologic ataxia
- Deafness hypogonadism syndrome
- Deafness hypospadias metacarpal and metatarsal syndrome
- Deafness mesenteric diverticula of small bowel neuropathy
- Deafness mixed with perilymphatic Gusher, X-linked
- Deafness nephritis ano rectal malformation
- Deafness neurosensory pituitary dwarfism
- Deafness nonsyndromic, Connexin 26 linked
- Deafness oligodontia syndrome
- Deafness onychodystrophy dominant form
- Deafness peripheral neuropathy arterial disease
- Deafness progressive cataract autosomal dominant
- Deafness skeletal dysplasia lip granuloma
- Deafness symphalangism
Deafness v-Deafness x
- Deafness vitiligo achalasia
- Deafness white hair contractures papillomas
- Deafness X-linked, DFN3
- Deafness, autosomal dominant nonsyndromic sensorineural
- Deafness, isolated, due to mitochondrial transmission
- Deafness, neurosensory nonsyndromic recessive, DFN
- Deafness, X linked, DFN
Deal
Dec-Del
- Deciduous skin
- Decompensated phoria
- Defect in synthesis of adenosylcobalamin
- Defective apolipoprotein B-100
- Defective expression of HLA class 2
- Degenerative motor system disease
- Degenerative optic myopathy
- Degos disease
- Degos 'en cocarde' erythrokeratoderma
- Dehydratase deficiency
- Dejerine-Sottas disease
- Delayed membranous cranial ossification
- Delayed speech facial asymmetry strabismus ear lobe creases
- Deletion 6q16 q21
- Delleman Oorthuys syndrome
- Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
- Delta-sarcoglycanopathy
Dem-Dep
- Dementia progressive lipomembranous polycysta
- Dementia, familial British
- Demodicidosis
- Demyelinating disease
- Dengue fever
- Dennis Cohen syndrome
- Dennis Fairhurst Moore syndrome
- Dent disease
- Dental aberrations steroid dehydrogenase deficienciency
- Dental fluorosis
- Dental tissue neoplasm
- Dentatorubral pallidoluysian atrophy
- Dentin dysplasia sclerotic bones
- Dentin dysplasia, coronal
- Dentin dysplasia, radicular
- Dentinogenesis imperfecta
- Dentophobia
- Depersonalization disorder
- Depression (clinical)
Der-Dev
- Dercum's disease aka Adiposis dolorosa
- Der kaloustian Jarudi Khoury syndrome
- Der Kaloustian Mcintosh Silver syndrome
- Dermal Dysplasia
- Dermatitis herpetiformis
- Dermatocardioskeletal syndrome Boronne type
- Dermatographic urticaria
- Dermatofibroma
- Dermatoleukodystrophy
- Dermatomyositis
- Dermatoosteolysis Kirghizian type
- Dermatopathia pigmentosa reticularis
- Dermatophytids
- Dermatophytosis
- Dermochondrocorneal dystrophy of François
- Dermoodontodysplasia
- Desbuquois syndrome
- Desmin related myopathy
- Desmoid disease
- Desmoid tumor
- Desmoplastic small round cell tumor
- Developmental delay hypotonia extremities hypertrophy
- Developmental dysphasia familial
- Devic syndrome
- Devriendt Legius Fryns syndrome
- Devriendt Vandenberghe Fryns syndrome
Dex
- Dexamethasone sensitive hypertension
- Dextrocardia with situs inversus
- Dextrocardia
- Dextrocardia-bronchiectasis-sinusitis
Dg
Di
Dia
Diab-Diam
- Diabetes hypogonadism deafness mental retardation
- Diabetes insipidus
- Diabetes insipidus, diabetes mellitus, optic atrophy
- Diabetes insipidus, nephrogenic type 1
- Diabetes insipidus, nephrogenic type 2
- Diabetes insipidus, nephrogenic type 3
- Diabetes insipidus, nephrogenic, dominant type
- Diabetes insipidus, nephrogenic, recessive type
- Diabetes mellitus
- Diabetes mellitus, transient neonatal
- Diabetes persistent mullerian ducts
- Diabetes, insulin dependent
- Diabetic angiopathy
- Diabetic embryopathy
- Diabetic nephropathy
- Diabetic neuropathy
- Diamond Blackfan disease
Diap-Dias
- Diaphragmatic agenesia
- Diaphragmatic agenesis radial aplasia omphalocele
- Diaphragmatic defect limb deficiency skull defect
- Diaphragmatic hernia abnormal face limb
- Diaphragmatic hernia exomphalos corpus callosum agenesis
- Diaphragmatic hernia upper limb defects
- Diaphragmatic hernia, congenital
- Diarrhea chronic with villous atrophy
- Diarrhea polyendocrinopathy infections X linked
- Diastematomyelia
- Diastrophic dysplasia
Dib-Din
- Dibasic aminoaciduria 2
- Dibasic aminoaciduria type 1
- Dicarboxylicaminoaciduria
- Die Smulders Droog Van Dijk syndrome
- Die Smulders Vles Fryns syndrome
- Diencephalic syndrome
- Dieterich's disease
- Diethylstilbestrol antenatal infection
- Diffuse idiopathic skeletal hyperostosis
- Diffuse leiomyomatosis with Alport syndrome
- Diffuse neonatal hemangiomatosis
- Diffuse palmoplantar keratoderma, Bothnian type
- Diffuse panbronchiolitis
- Diffuse parenchymal lung disease
- DiGeorge syndrome
- Digestive duplication
- Digitorenocerebral syndrome
- Dihydropteridine reductase deficiency
- Dihydropyrimidine dehydrogenase deficiency
- Dilated cardiomyopathy
- Dimitri Sturge Weber syndrome
- Dincsoy Salih Patel syndrome
- Dinno Shearer Weisskopf syndrome
Dio-Dip
- Diomedi Bernardi Placidi syndrome
- Dionisi Vici Sabetta Gambarara syndrome
- Diphallia
- Diphallus rachischisis imperforate anus
- Diphosphoglycerate mutase deficiency of erythrocyte
- Diphtheria
Dis-Div
- Disaccharide intolerance iii
- Discoid lupus erythematosus
- Dislocation of the hip dysmorphism
- Disorder in the hormonal synthesis with or without goiter
- Disorganization syndrome
- Dissecting cellulitis of the scalp
- Dissociative amnesia
- Dissociative hysteria
- Dissociative fugue
- Dissociative identity disorder
- Distal arthrogryposis Moore Weaver type
- Distal myopathy Markesbery-Griggs type
- Distal myopathy with vocal cord weakness
- Distal myopathy, Nonaka type
- Distal myopathy
- Distal primary acidosis, familial
- Distemper
- Distichiasis heart congenital anomalies
- Distomatosis
- Diverticulitis
- Diverticulosis
Dk-Do
- Dk phocomelia syndrome
- D-minus hemolytic uremic syndrome
- Dobrow syndrome
- Dominant cleft palate
- Dominant ichthyosis vulgaris
- Dominant zonular cataract
- Donnai Barrow syndrome
- Door syndrome
- Dopamine beta-hydroxylase deficiency
- DOPA-responsive dystonia
- Double cortex
- Double discordia
- Double fingernail of fifth finger
- Double outlet left ventricle
- Double outlet right ventricle
- Double tachycardia induced by catecholamines
- Double uterus-hemivagina-renal agenesis
- Downs Syndrome
- Doxorubicin-induced cardiomyopathy
- Doyne honeycomb retinal dystrophy
Dp-Du
- D-plus hemolytic uremic syndrome
- Drachtman Weinblatt Sitarz syndrome
- Dracunculiasis
- Duane anomaly mental retardation
- Duane syndrome
- Dubin-Johnson syndrome
- Dubowitz syndrome
- Duchenne muscular dystrophy
- Duhring Brocq disease
- Duhring's disease
- Duker Weiss Siber syndrome
- Duodenal atresia tetralogy of Fallot
- Duodenal atresia
- Duplication of leg mirror foot
- Duplication of the thumb unilateral biphalangeal
- Duplication of urethra
- Dupont Sellier Chochillon syndrome
- Dupuytren subungual exostosis
- Dupuytren's contracture
- Dust-induced lung disease
Dw
- Dwarfism bluish sclerae
- Dwarfism deafness retinitis pigmentosa
- Dwarfism lethal type advanced bone age
- Dwarfism mental retardation eye abnormality
- Dwarfism short limb absent fibulas very short digits
- Dwarfism stiff joint ocular abnormalities
- Dwarfism syndesmodysplasic
- Dwarfism tall vertebrae
- Dwarfism thanatophoric
- Dwarfism thin bones multiple fractures
- Dwarfism
Dy
Dyg-Dyk
Dys
Dysa-Dysk
- Dysautonomia (does not have to be familial) (Autonomic Nervous System Diseases)
- Dysbarism
- Dyschondrosteosis nephritis
- Dyschromatosis universalis
- Dysencephalia splachnocystica or Meckel Gruber
- Dysequilibrium syndrome
- Dyserythropoietic anemia, congenital type 1
- Dyserythropoietic anemia, congenital type 2
- Dyserythropoietic anemia, congenital type 3
- Dyserythropoietic anemia, congenital
- Dysferlinopathy
- Dysfibrinogenemia, familial
- Dysgerminoma
- Dysharmonic skeletal maturation muscular fiber disproportion
- Dyskeratosis congenita of Zinsser Cole Engman
- Dyskeratosis congenita
- Dyskeratosis follicularis
- Dyskinesia, drug induced
- Dyskinesia
Dysm-Dyss
- Dysmorphism abnormal vocalization mental retardation
- Dysmorphism cleft palate loose skin
- Dysmorphophobia
- Dysmyelination
- Dysosteosclerosis
- Dysostosis acral with facial and genital abnormalities
- Dysostosis peripheral
- Dysostosis Stanescu type
- Dysostosis
- Dysphasic dementia, hereditary
- Dysphonia, chronic spasmodic
- Dysplasia epiphysealis hemimelica
- Dysplasia
- Dysplastic cortical hyperostosis
- Dysplastic nevus syndrome
- Dysprothrombinemia
- Dysraphism cleft lip palate limb reduction defects
- Dyssegmental dysplasia glaucoma
- Dyssegmental dysplasia Silverman Handmaker type
Dyst
- Dysthymia
- Dystonia musculorum deformans type 1
- Dystonia musculorum deformans type 2
- Dystonia musculorum deformans
- Dystonia progressive with diurnal variation
- Dystonia
- Dystrophia myotonica
- Dystrophic epidermolysis bullosa
- Dystrophinopathy
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
