Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/4
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- 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
- Daneman Davy Mancer syndrome
- Davenport Donlan syndrome
- David syndrome
- Davis Lafer syndrome
- 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 '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
- Dementia progressive lipomembranous polycysta
- Dementia, familial British
- Demodicidosis
- Dennis Cohen syndrome
- Dennis Fairhurst Moore syndrome
- Dent disease
- Dental aberrations steroid dehydrogenase deficienciency
- Dental tissue neoplasm
- Dentatorubral pallidoluysian atrophy
- Dentin dysplasia sclerotic bones
- Dentin dysplasia, coronal
- Dentin dysplasia, radicular
- Der kaloustian Jarudi Khoury syndrome
- Der Kaloustian Mcintosh Silver syndrome
- Dercum's disease
- Dermatocardioskeletal syndrome Boronne type
- Dermatoleukodystrophy
- Dermatoosteolysis Kirghizian type
- Dermatopathia pigmentosa reticularis
- Dermatophytids
- Dermochondrocorneal dystrophy of François
- Dermoodontodysplasia
- Desbuquois syndrome
- Desmin related myopathy
- Desmoid disease
- Desmoid tumor
- Developmental delay hypotonia extremities hypertrophy
- Developmental dysphasia familial
- Devic syndrome
- Devriendt Legius Fryns syndrome
- Devriendt Vandenberghe Fryns syndrome
- Dexamethasone sensitive hypertension
- Dextrocardia-bronchiectasis-sinusitis
- D-glycerate dehydrogenase deficiency
- D-glycericacidemia
- 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
- Diabetic embryopathy
- 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
- Diarrhea chronic with villous atrophy
- Diarrhea polyendocrinopathy infections X linked
- Diastematomyelia
- Dibasic aminoaciduria type 1
- Dicarboxylicaminoaciduria
- Die Smulders Droog Van Dijk syndrome
- Die Smulders Vles Fryns syndrome
- Diencephalic syndrome
- Dieterich's disease
- Diffuse idiopathic skeletal hyperostosis
- Diffuse leiomyomatosis with Alport syndrome
- Diffuse neonatal hemangiomatosis
- Diffuse palmoplantar keratoderma, Bothnian type
- Diffuse panbronchiolitis
- Digestive duplication
- Digitorenocerebral syndrome
- Dihydropteridine reductase deficiency
- Dihydropyrimidine dehydrogenase deficiency
- Dimitri Sturge Weber syndrome
- Dincsoy Salih Patel syndrome
- Dinno Shearer Weisskopf syndrome
- Diomedi Bernardi Placidi syndrome
- Dionisi Vici Sabetta Gambarara syndrome
- Diphallus rachischisis imperforate anus
- Diphosphoglycerate mutase deficiency of erythrocyte
- Disaccharide intolerance iii
- 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
- D-minus hemolytic uremic syndrome
- Dobrow syndrome
- Dominant cleft palate
- 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 tachycardia induced by catecholamines
- Double uterus-hemivagina-renal agenesis
- Doyne honeycomb retinal dystrophy
- D-plus hemolytic uremic syndrome
- Drachtman Weinblatt Sitarz syndrome
- Duane anomaly mental retardation
- 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
- 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
- Dyggve-Melchior-Clausen syndrome
- Dykes Markes Harper syndrome
- 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
- Dysharmonic skeletal maturation muscular fiber disproportion
- Dyskeratosis congenita of Zinsser Cole Engman
- Dyskeratosis follicularis
- Dysmorphism abnormal vocalization mental retardation
- Dysmorphism cleft palate loose skin
- Dysmyelination
- Dysosteosclerosis
- Dysostosis acral with facial and genital abnormalities
- Dysostosis peripheral
- Dysostosis Stanescu type
- Dysostosis
- Dysphasic dementia, hereditary
- Dysphonia, chronic spasmodic
- Dysplasia epiphysealis hemimelica
- Dysplastic cortical hyperostosis
- Dysprothrombinemia
- Dysraphism cleft lip palate limb reduction defects
- Dyssegmental dysplasia glaucoma
- Dyssegmental dysplasia Silverman Handmaker type
- Dystonia musculorum deformans type 1
- Dystonia musculorum deformans type 2
- Dystonia musculorum deformans
- Dystonia progressive with diurnal variation
- Dystrophia myotonica
- Dystrophic epidermolysis bullosa
- Dystrophinopathy
- Ear, patella, short stature syndrome
- Earlobes thickened conductive deafness
- Eccentrochondrodysplasia
- Eccrine acrospiroma
- Ecp syndrome
- Ectodermal dysplasia absent dermatoglyphics
- Ectodermal dysplasia adrenal cyst
- Ectodermal dysplasia alopecia preaxial polydactyly
- Ectodermal dysplasia anhidrotic
- Ectodermal dysplasia arthrogryposis diabetes mellitus
- Ectodermal dysplasia Bartalos type
- Ectodermal dysplasia Berlin type
- Ectodermal dysplasia blindness
- Ectodermal dysplasia ectrodactyly macular dystrophy
- Ectodermal dysplasia hypohidrotic autosomal dominant
- Ectodermal dysplasia hypohidrotic hypothyroidism ciliary diskinesia
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation CNS malformation
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia neurosensory deafness
- Ectodermal dysplasia osteosclerosis
- Ectodermal dysplasia tricho odonto onychial type
- Ectodermal dysplasia, hydrotic
- Ectodermal dysplasia, hypohidrotic, autosomal recessive
- Ectodermal dysplasias
- Ectodermic dysplasia anhidrotic cleft lip
- Ectopia lentis isolated
- Ectopia pupillae
- Ectopic coarctation
- Ectopic ossification familial type
- Ectrodactyly cardiopathy dysmorphism
- Ectrodactyly cleft palate syndrome
- Ectrodactyly diaphragmatic hernia corpus callosum
- Ectrodactyly dominant form
- Ectrodactyly ectrodermal dysplasia
- Ectrodactyly polydactyly
- Ectrodactyly recessive form
- Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate
- Ectropion inferior cleft lip and or palate
- Edinburgh malformation syndrome
- Edwards Patton Dilly syndrome
- Eec syndrome without cleft lip palate
- Eec syndrome
- Eem syndrome
- Egg shaped pupils
- Eijkman's syndrome
- Eisenmenger syndrome
- Elattoproteus in context of NF
- Electron transfer flavoprotein, deficiency of
- Elejalde syndrome
- Elliott Ludman Teebi syndrome
- Ellis Yale Winter syndrome
- Emerinopathy
- Emery Nelson syndrome
- Emery-Dreifuss muscular dystrophy, dominant type
- Emery-Dreifuss muscular dystrophy, X-linked
- Emery-Dreifuss muscular dystrophy
- Emphysema, congenital lobar
- Emphysema-penoscrotal web-deafness-mental retardation
- Enamel hypoplasia cataract hydrocephaly
- Encephalo cranio cutaneous lipomatosis
- Encephalocele anterior
- Encephalocele frontal
- Encephalopathy intracerebral calcification retinal
- Encephalopathy progressive optic atrophy
- Encephalopathy subacute spongiform, Gerstmann-Stra
- Encephalopathy-basal ganglia-calcification
- Encephalophathy recurrent of childhood
- Encephalotrigeminal angiomatosis
- Enchondromatosis (benign)
- Enchondromatosis dwarfism deafness
- Endocardial fibroelastosis
- Endometrial stromal sarcoma
- Endomyocardial fibroelastosis
- Eng Strom syndrome
- Engelhard Yatziv syndrome
- Englemann disease
- Enolase deficiency type 1
- Enolase deficiency type 2
- Enolase deficiency type 3
- Enolase deficiency type 4
- Enolase deficiency
- Enteropathica
- Enterovirus antenatal infection
- Environment associated hypertension
- Eosinophilic cryptitis
- Eosinophilic cystitis
- Eosinophilic gastroenteritis
- Eosinophilic granuloma
- Eosinophilic lymphogranuloma
- Eosinophilic Pustular Folliculitis
- Eosinophilic synovitis
- Ependymoblastoma
- Epidemic encephalitis
- Epidemic encephalomyelitis
- Epidermal nevus vitamin D resistant rickets
- Epidermodysplasia verruciformis
- Epidermoid carcinoma
- Epidermolysa bullosa simplex and limb girdle muscular dystrophy
- Epidermolysis bullosa acquisita
- Epidermolysis bullosa dystrophica, Bart type
- Epidermolysis bullosa dystrophica, dominant type
- Epidermolysis bullosa herpetiformis, Dowling-Meara
- Epidermolysis bullosa intraepidermic
- Epidermolysis bullosa inversa dystrophica
- Epidermolysis bullosa simplex with anodontia, hair
- Epidermolysis bullosa simplex, Cockayne-Touraine type
- Epidermolysis bullosa simplex, Koebner type
- Epidermolysis bullosa simplex, Ogna type
- Epidermolysis bullosa, dermolytic
- Epidermolysis bullosa, generalized atrophic benign
- Epidermolysis bullosa, junctional, Herlitz-Pearson
- Epidermolysis bullosa, junctional, with pyloric atrophy
- Epidermolysis bullosa, junctional
- Epidermolysis bullosa, pretibial
- Epidermolytic palmoplantar keratoderma Vorner type
- Epilepsy benign neonatal dominant form
- Epilepsy benign neonatal recessive form
- Epilepsy mental deterioration Finnish type
- Epilepsy microcephaly skeletal dysplasia
- Epilepsy occipital calcifications
- Epilepsy progressive myoclonic type 2
- Epilepsy telangiectasia
- Epilepsy with myoclono-astatic crisis
- Epilepsy, benign occipital
- Epilepsy, myoclonic progressive familial
- Epilepsy, nocturnal, frontal lobe type
- Epilepsy, partial, familial
- Epimerase deficiency
- Epimetaphyseal dysplasia cataract
- Epimetaphyseal skeletal dysplasia
- Epiphyseal dysplasia dysmorphism camptodactyly
- Epiphyseal dysplasia hearing loss dysmorphism
- Epiphyseal dysplasia multiple
- Epiphysealis hemimelica dysplasia
- Epithelial-myoepithelial carcinoma
- Epitheliopathy (APMPPE)
- Epitheliopathy, acute posterior multifocal placoid
- Epstein syndrome
- Erb-Duchenne palsy
- Erdheim disease
- Eronen Somer Gustafsson syndrome
- Erosive pustular dermatosis of the scalp
- Erythroderma desquamativa of Leiner
- Erythroderma lethal congenital
- Erythrokeratodermia ataxia
- Erythrokeratodermia progressive symmetrica ichthyosis
- Erythrokeratodermia symmetrica progressiva
- Erythrokeratodermia variabilis ichthyosis
- Erythrokeratodermia variabilis, Mendes da Costa type
- Erythrokeratodermia with ataxia
- Erythrokeratolysis hiemalis ichthyosis
- Escher Hirt syndrome
- Esophageal atresia associated anomalies
- Esophageal atresia coloboma talipes
- Esophageal duodenal atresia abnormalities of hands
- Essential iris atrophy
- Essential mixed cryoglobulinemia
- Esthesioneuroblastoma
- Ethylmalonic aciduria
- Ethylmalonic adipic aciduria
- Euhidrotic ectodermal dysplasia
- Eunuchoidism familial
- Exercise induced anaphylaxis
- Exfoliative dermatitis
- Exner syndrome
- Exomphalos-macroglossia-gigantism syndrome
- Exostoses anetodermia brachydactyly type E
- Experimental allergic encephalomyelitis
- Extrasystoles short stature hyperpigmentation microcephaly
- Exudative retinopathy familial, autosomal dominant
- Exudative retinopathy familial, autosomal recessive
- Exudative retinopathy familial, X linked, recessive
- Exudative retinopathy, familial
- Eye defects arachnodactyly cardiopathy
- Eyebrows duplication syndactyly
