List of rare diseases starting with D

This list of rare diseases was originally taken from the NIH public domain resource at http://ord.aspensys.com/asp/diseases/diseases.asp .

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

Table of contents

1 Da-Dd
2 De-Dh
3 Di-Dl
4 Dm-Dp
5 Dq-Dt
6 Du-Dz

Da-Dd

D ercole syndrome
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-Dh

De Barsy syndrome
De Hauwere Leroy Adriaenssens syndrome
De Sanctis-Cacchione syndrome
Deaf blind hypopigmentation
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 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 Barratt Dillon syndrome
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
Deipnophobia
Dejerine-Sottas disease
Delayed membranous cranial ossification
Delayed speech facial asymetry strabismus ear lobe creases
Deletion 6q16 q21
Delleman Oorthuys syndrome
Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
Delta-sarcoglycanopathy
Dementia progressive lipomembranous polycysta
Dementia, familial british
Dementophobia
Demodicidosis
Demonophobia
Demyelinating diseases
Dendrophobia
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
Der kaloustian Jarudi Khoury syndrome
Der Kaloustian Mcintosh Silver syndrome
Dermatitis herpetiformis
Dermatocardioskeletal syndrome Boronne type
Dermatographic uticaria
Dermatoleukodystrophy
Dermatomyositis
Dermatoosteolysis Kirghizian type
Dermatopathia pigmentosa reticularis
Dermatophobia
Dermochondrocorneal dystrophy of Fran�ois
Dermoodontodysplasia
Desbuquois syndrome
Desmin related myopathy
Desmoid disease
Desmoid tumor
Desmoplastic small cell tumor
Developmental delay hypotonia extremities hypertrophy
Developmental dysphasia familial
Devic syndrome
Devriendt Legius Fryns syndrome
Devriendt Vandenberghe Fryns syndrome
Dexamethasone sensitive hypertension
Dextrocardia with situs inversus
Dextrocardia
Dextrocardia-bronchiectasis-sinusitis
D-glycerate dehydrogenase deficiency
D-glycericacidemia

Di-Dl

Diabetes hypogonadism deafness mental retardation
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, transient neonatal
Diabetes persistent mullerian ducts
Diabetes, insulin dependent
Diabetic angiopathy
Diabetic embryopathy
Diabetic nephropathy
Diabetic neuropathy
Diamond Blackfan disease
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
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
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
Dinophobia
Diomedi Bernardi Placidi syndrome
Dionisi Vici Sabetta Gambarara syndrome
Diphallia
Diphallus rachischisis imperforate anus
Diphosphoglycerate mutase deficiency of erythrocyte
Diphtheria
Diplophobia
Diprosopia
Dipsophobia
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 hysteria
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
Distichiasis heart congenital anomalies
Distomatosis
Diverticulitis
Diverticulosis
Dk phocomelia syndrome

Dm-Dp

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
Doraphobia
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
D-plus hemolytic uremic syndrome

Dq-Dt

Drachtman Weinblatt Sitarz syndrome
Dracunculiasis

Du-Dz

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
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
Dyggve-Melchior-Clausen syndrome
Dykes Markes Harper syndrome
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
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
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
Dystychiphobia