List of rare diseases/D

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

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 François
• 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

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