List of diseases (D): Difference between revisions
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Latest revision as of 16:56, 9 August 2012
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