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D-TGA ( Transposition of the great arteries, dextro-looped 1 [5] )
D-glycerate dehydrogenase deficiency ( Hyperoxaluria, primary, type II [2] )
DA2A ( Freeman-Sheldon syndrome [16] )
DA2B ( Arthrogryposis, distal, type 2B [3] )
DAR ( Darier disease [43] )
DBA ( Diamond-Blackfan anemia [4] )
DBQD ( Desbuquois syndrome [1] )
DCO ( Leri-Weill dyschondrosteosis [6] )
DCR ( Trisomy 21 [21] )
DCS ( Triglyceride storage disease with impaired long-chain fatty acid oxidation [7] )
DCWHK ( Carvajal syndrome [3] )
DDD ( Dowling-Degos disease [10] )
DDEB ( Epidermolysis bullosa dystrophica, autosomal dominant [2] )
DDP ( Mohr-Tranebjaerg syndrome [1] )
DDPAC ( Frontotemporal dementia [63] )
DDS ( Mohr-Tranebjaerg syndrome [1] )
DDSH ( Dyssegmental dysplasia, Silverman-Handmaker type [1] )
DEB, pretibial ( Epidermolysis bullosa dystrophica, pretibial [3] )
DEB, pruriginosa ( Epidermolysis bullosa pruriginosa [8] )
DEND ( Diabetes mellitus, permanent neonatal [1] )
DES ( Cerebellar hypoplasia, VLDLR-associated [1] )
DES ( Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion: CHMRQ1 [1] )
DES exposure ( Diethylstilbestrol exposure [6] )
DFN3 ( Deafness, X-linked 2 [5] )
DFNA9 ( Deafness, autosomal dominant nonsyndromic sensorineural 9 [1] )
DFNB4 ( Enlarged vestibular aqueduct [1] )
DFNB53 ( Deafness, autosomal recessive 53 [1] )
DFNX2 ( Deafness, X-linked 2 [5] )
DGI-II ( Dentinogenesis imperfecta 1 [21] )
DGI1 ( Dentinogenesis imperfecta 1 [21] )
DGS ( DiGeorge syndrome [13] )
DGSX ( Simpson-Golabi-Behmel syndrome [2] )
DHOF ( Focal dermal hypoplasia [10] )
DHRD ( Doyne honeycomb retinal dystrophy [7] )
DHTR deficiency ( Androgen insensitivity syndrome [21] )
DIAR2 ( Microvillus inclusion disease [10] )
DIDMOAD ( Wolfram syndrome 1 [1] )
DJS ( Dubin-Johnson syndrome [2] )
DK phocomelia syndrome [1]
DK1 deficiency ( Combined oxidative phosphorylation deficiency 1 [2] )
DKBI ( Dyskeratosis, hereditary benign intraepithelial [4] )
DLD deficiency ( Maple syrup urine disease [7] )
DM ( Dystrophia myotonica [16] )
DM1 ( Dystrophia myotonica [16] )
DM2 ( Dystrophia myotonica 2 [6] )
DMC ( Dyggve-Melchior-Clausen disease [3] )
DMD ( Duchenne muscular dystrophy [17] )
DMRV ( Nonaka myopathy [9] )
DMSD ( Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked [2] )
DMSMFH ( Diaphyseal medullary stenosis with malignant fibrous histiocytoma [2] )
DPD deficiency ( Dihydropyrimidine dehydrogenase deficiency [3] )
DPD1 ( Camurati-Engelmann disease [16] )
DR syndrome ( Duane radial ray syndrome [11] )
DRM ( Myopathy, myofibrillar, desmin-related [13] )
DRPLA ( Dentatorubral-pallidoluysian atrophy [2] )
DRRS ( Duane radial ray syndrome [11] )
DRS ( Duane retraction syndrome 1 [11] )
DSAP ( Porokeratosis, disseminated superficial actinic, 1 [8] )
DSAP1 ( Porokeratosis, disseminated superficial actinic, 1 [8] )
DSCR ( Trisomy 21 [21] )
DSH1 ( Dyschromatosis symmetrica hereditaria [5] )
DSMAV ( Spinal muscular atrophy, distal, type V [4] )
DSMAX ( Spinal muscular atrophy, distal, X-linked recessive [1] )
DSN ( Dejerine-Sottas syndrome [10] )
DSS ( Dejerine-Sottas syndrome [10] )
DTD ( Diastrophic dysplasia [10] )
DTDP2 ( Dentin dysplasia, type II [1] )
DTGA1 ( Transposition of the great arteries, dextro-looped 1 [5] )
DUH ( Dyschromatosis universalis hereditaria [12] )
DURS1 ( Duane retraction syndrome 1 [11] )
DURS2 ( Duane retraction syndrome 2 [1] )
DUS ( Duane retraction syndrome 1 [11] )
DVA ( Enlarged vestibular aqueduct [1] )
DWS ( Dandy-Walker syndrome [23] )
DYS ( Neuropathy, hereditary sensory and autonomic, type III [4] )
Dacryocystocele [10]
Dandy-Walker malformation ( Dandy-Walker syndrome [23] )
Dandy-Walker syndrome [23]
Dandy-Walker syndrome - Prenatal diagnosis [12]
Danon disease [11]
Dappled metaphysis syndrome ( Spondyloepimetaphyseal dysplasia, Strudwick type [2] )
Darier disease [43]
Darier-White disease ( Darier disease [43] )
Dauwerse-Peters syndrome [3]
Davidson disease ( Microvillus inclusion disease [10] )
De Morsier syndrome ( Septooptic dysplasia [28] )
Deafness 3, conductive, with stapes fixation ( Deafness, X-linked 2 [5] )
Deafness syndrome, progressive, with blindness, dystonia, fractures, and mental deficiency ( Mohr-Tranebjaerg syndrome [1] )
Deafness with goiter ( Pendred syndrome [8] )
Deafness, X-linked 2 [5]
Deafness, autosomal dominant nonsyndromic sensorineural 9 [1]
Deafness, autosomal recessive 4 ( Enlarged vestibular aqueduct [1] )
Deafness, autosomal recessive 53 [1]
Deafness, conductive, with stapes fixation ( Deafness, X-linked 2 [5] )
Deafness, congenital, and functional heart disease ( Jervell and Lange-Nielsen syndrome [3] )
Deafness, congenital, and split hands and feet ( Split-hand/foot malformation with sensorineural hearing loss [3] )
Deafness, congenital, with inner ear agenesis, microtia, and microdontia [4]
Deafness, congenital, with keratopachydermia and constrictions of fingers and toes ( Vohwinkel syndrome [16] )
Deafness, mixed, with perilymphatic gusher ( Deafness, X-linked 2 [5] )
Deafness, sensorineural, with imperforate anus and thumb anomalies ( Townes-Brocks syndrome [11] )
Deafness-dystonia-optic atrophy syndrome ( Mohr-Tranebjaerg syndrome [1] )
Deafness-imperforate anus-hypoplastic thumbs syndrome ( Townes-Brocks syndrome [11] )
Defect11 syndrome ( Potocki-Shaffer syndrome [2] )
Degos disease ( Malignant atrophic papulosis [12] )
Dejerine-Sottas neuropathy ( Dejerine-Sottas syndrome [10] )
Dejerine-Sottas syndrome [10]
Del Castillo syndrome ( Sertoli cell-only syndrome [17] )
Deletion 1p36 ( Monosomy 1p36 syndrome [3] )
Deletion 3p syndrome [1]
Deletion 5p ( Cri-du-chat syndrome [8] )
Delleman syndrome ( Oculocerebrocutaneous syndrome [7] )
Delta storage pool disease ( Hermansky-Pudlak syndrome [21] )
Dementia, frontotemporal, with parkinsonism ( Frontotemporal dementia [63] )
Dementia, hereditary dysphasic disinhibition ( Frontotemporal lobar degeneration with ubiquitin-positive inclusions [25] )
Dementia, hereditary multi-infarct type ( Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy [49] )
Dementia, prefrontal, with bone cysts ( Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [3] )
Dementia, progressive, with lipomembranous polycystic osteodysplasia ( Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [3] )
Demyer sequence ( Holoprosencephaly 2 [2] )
Dent disease 1 [2]
Dental transposition [4]
Dentatorubral-pallidoluysian atrophy [2]
Dentin dysplasia, Shields type II ( Dentin dysplasia, type II [1] )
Dentin dysplasia, type I [1]
Dentin dysplasia, type II [1]
Dentinogenesis imperfecta [6]
Dentinogenesis imperfecta 1 [21]
Dentinogenesis imperfecta without osteogenesis imperfecta ( Dentinogenesis imperfecta 1 [21] )
Dentinogenesis imperfecta, Shields type II ( Dentinogenesis imperfecta 1 [21] )
Denys-Drash syndrome [8]
Depressor anguli oris muscle hypoplasia ( Hypoplasia of the depressor anguli oris muscle [5] )
Dermal sinus tract [3]
Dermatofibrosis lenticularis disseminata with osteopoikilosis ( Buschke-Ollendorff syndrome [4] )
Dermatofibrosis, disseminated, with osteopoikilosis ( Buschke-Ollendorff syndrome [4] )
Dermatoosteopoikilosis ( Buschke-Ollendorff syndrome [4] )
Desbuquois syndrome [1]
Desmin-related myopathy ( Myopathy, myofibrillar, desmin-related [13] )
Desmin-related myopathy with Mallory bodies ( Rigid spine muscular dystrophy 1 [5] )
Desminopathy, primary ( Myopathy, myofibrillar, desmin-related [13] )
Desquamation of newborn ( Ichthyosis congenita [21] )
Desquamative interstitial pneumonitis due to surfactant protein C deficiency ( Surfactant metabolism dysfunction, pulmonary, 2 [3] )
Developmental delay and recurrent infections [1]
Developmental delay, epilepsy, and neonatal diabetes ( Diabetes mellitus, permanent neonatal [1] )
Dextrocardia, bronchiectasis, and sinusitis ( Kartagener syndrome [12] )
DiGeorge syndrome [13]
Diabetes insipidus and mellitus with optic atrophy and deafness ( Wolfram syndrome 1 [1] )
Diabetes insipidus, cranial type ( Diabetes insipidus, neurohypophyseal type [2] )
Diabetes insipidus, nephrogenic, X-linked [1]
Diabetes insipidus, nephrogenic, type I ( Diabetes insipidus, nephrogenic, X-linked [1] )
Diabetes insipidus, neurohypophyseal type [2]
Diabetes insipidus, primary central ( Diabetes insipidus, neurohypophyseal type [2] )
Diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea ( Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked [2] )
Diabetes mellitus, permanent neonatal [1]
Diabetes mellitus, permanent neonatal, with cerebellar agenesis [3]
Diabetes mellitus, permanent neonatal, with neurologic features ( Diabetes mellitus, permanent neonatal [1] )
Diabetes mellitus, permanent, of infancy ( Diabetes mellitus, permanent neonatal [1] )
Diabetic embryopathy [12]
Diabetic fetopathy ( Diabetic embryopathy [12] )
Diamond-Blackfan anemia [4]
Diaphragm agenesis ( Diaphragmatic agenesis [8] )
Diaphragmatic agenesis [8]
Diaphragmatic hernia [53]
Diaphragmatic hernia - Prenatal diagnosis [19]
Diaphragmatic hernia repair [13]
Diaphragmatic hernia, abnormal face, and distal limb anomalies ( Fryns syndrome [5] )
Diaphragmatic hernia, congenital ( Diaphragmatic hernia [53] )
Diaphyseal aclasis ( Exostoses, multiple [57] )
Diaphyseal dysplasia 1, progressive ( Camurati-Engelmann disease [16] )
Diaphyseal medullary stenosis with malignant fibrous histiocytoma [2]
Diarrhea 2, with microvillous atrophy ( Microvillus inclusion disease [10] )
Diarrhea, congenital secretory, chloride type ( Chloride diarrhea, familial [2] )
Diarrhea, fatal infantile, with trichorrhexis nodosa ( Trichohepatoenteric syndrome [4] )
Diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked ( Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked [2] )
Diarrhea, syndromic ( Trichohepatoenteric syndrome [4] )
Diastematomyelia [27]
Diastematomyelia - Prenatal diagnosis [3]
Diastrophic dysplasia [10]
Dibasicamino aciduria II ( Lysinuric protein intolerance [2] )
Diethylstilbestrol exposure [6]
Diffuse leiomyomatosis with Alport syndrome ( Alport syndrome and diffuse leiomyomatosis [3] )
Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum ( Feingold syndrome [5] )
Dihydrolipoamide dehydrogenase deficiency ( Maple syrup urine disease [7] )
Dihydropyrimidine dehydrogenase deficiency [3]
Dihydrotestosterone receptor deficiency ( Androgen insensitivity syndrome [21] )
Dilated vestibular aqueduct ( Enlarged vestibular aqueduct [1] )
Diphallia ( Diphallus [3] )
Diphallus [3]
Diploid/triploid mixoploidy ( Diploid/triploid mosaicism [1] )
Diploid/triploid mosaicism [1]
Diprosopus ( Conjoined twins, diprosopus [53] )
Disaccharide intolerance I [1]
Disinhibition-dementia-parkinsonism-amyotrophy complex ( Frontotemporal dementia [63] )
Disordered steroidogenesis ( POR deficiency [2] )
Disorganization-like syndrome [1]
Dohle leukocyte inclusions with giant platelets ( May-Hegglin anomaly [14] )
Dolichol kinase deficiency ( Congenital disorder of glycosylation, type Im [1] )
Donohue syndrome ( Leprechaunism [5] )
Dorfman-Chanarin syndrome ( Triglyceride storage disease with impaired long-chain fatty acid oxidation [7] )
Double aortic arch ( Aortic arch, double [55] )
Double cortex syndrome ( Lissencephaly, X-linked [2] )
Double gallbladder ( Gallbladder duplication [2] )
Double uterus ( Uterus didelphys [34] )
Dowling-Degos disease [10]
Dowling-Degos-Kitamura disease ( Dowling-Degos disease [10] )
Down syndrome ( Trisomy 21 [21] )
Down syndrome chromosome region ( Trisomy 21 [21] )
Down syndrome critical region ( Trisomy 21 [21] )
Doyne honeycomb degeneration of retina ( Doyne honeycomb retinal dystrophy [7] )
Doyne honeycomb retinal dystrophy [7]
Drash syndrome ( Denys-Drash syndrome [8] )
Drusen, radial, autosomal dominant ( Doyne honeycomb retinal dystrophy [7] )
Du Pan syndrome ( Fibular hypoplasia and complex brachydactyly [2] )
Duane anomaly ( Duane retraction syndrome 1 [11] )
Duane anomaly with radial ray abnormalities and deafness ( Duane radial ray syndrome [11] )
Duane radial ray syndrome [11]
Duane retraction syndrome 1 [11]
Duane retraction syndrome 2 [1]
Duane syndrome ( Duane retraction syndrome 1 [11] )
Dubin-Johnson syndrome [2]
Dubowitz syndrome [2]
Duchenne muscular dystrophy [17]
Duchenne muscular dystrophy - Histology [27]
Duncan disease ( Lymphoproliferative syndrome, X-linked [5] )
Dunnigan-Kobberling syndrome ( Lipodystrophy, familial partial [7] )
Duodenal atresia [17]
Duodenal duplication [19]
Duplication 17p11.2 syndrome ( Potocki-Lupski syndrome [1] )
Duplication of the penis ( Diphallus [3] )
Dupuytren contracture [3]
Dural sinus malformation [3]
Dwarfism of Sindh [3]
Dwarfism with stiff joints and ocular abnormalities ( Moore-Federman syndrome [4] )
Dwarfism, diastrophic ( Diastrophic dysplasia [10] )
Dwarfism, geleophysic ( Geleophysic dysplasia [5] )
Dwarfism, metatropic ( Metatropic dwarfism [2] )
Dyggve-Melchior-Clausen disease [3]
Dyggve-Melchior-Clausen syndrome ( Dyggve-Melchior-Clausen disease [3] )
Dysautonomia, familial ( Neuropathy, hereditary sensory and autonomic, type III [4] )
Dysbetalipoproteinemia ( Hyperlipoproteinemia, type III [6] )
Dyschondroplasia ( Enchondromatosis [5] )
Dyschondrosteosis ( Leri-Weill dyschondrosteosis [6] )
Dyschondrosteosis, homozygous ( Langer mesomelic dysplasia [7] )
Dyschromatosis symmetrica hereditaria [5]
Dyschromatosis symmetrica hereditaria 1 ( Dyschromatosis symmetrica hereditaria [5] )
Dyschromatosis universalis hereditaria [12]
Dysencephalia splanchnocystica ( Meckel syndrome [4] )
Dysequilibrium syndrome ( Cerebellar hypoplasia, VLDLR-associated [1] )
Dysequilibrium syndrome ( Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion: CHMRQ1 [1] )
Dyserythropoietic anemia with thrombocytopenia [6]
Dyserythropoietic anemia, congenital, type I ( Anemia, dyserythropoietic congenital, type I [1] )
Dysgenetic male pseudohermaphroditism [5]
Dyskeratosis congenita [17]
Dyskeratosis congenita, Scoggins type ( Dyskeratosis congenita, autosomal dominant [2] )
Dyskeratosis congenita, X-linked [4]
Dyskeratosis congenita, autosomal dominant [2]
Dyskeratosis, hereditary benign intraepithelial [4]
Dysosteosclerosis [3]
Dysplasia epiphysealis hemimelica [13]
Dysplasia gigantism syndrome, X-linked ( Simpson-Golabi-Behmel syndrome [2] )
Dysplasia of nails with hypodontia ( Witkop syndrome [15] )
Dysplasia olfactogenitalis of de Morsier ( Kallmann syndrome 1 [2] )
Dysplastic gangliocytoma of the cerebellum ( Cowden disease [22] )
Dysplastic nevus syndrome, hereditary ( Melanoma, cutaneous malignant [14] )
Dyssegmental dysplasia, Silverman-Handmaker type [1]
Dystonia, alcohol-responsive ( Myoclonic dystonia [2] )
Dystonia-deafness syndrome ( Mohr-Tranebjaerg syndrome [1] )
Dystrophia brevicollis congenita ( Klippel-Feil syndrome [20] )
Dystrophia myotonica [16]
Dystrophia myotonica 1 ( Dystrophia myotonica [16] )
Dystrophia myotonica 2 [6]
Dystrophic epidermolysis bullosa pruriginosa ( Epidermolysis bullosa pruriginosa [8] )
Dystrophic epidermolysis bullosa, autosomal dominant ( Epidermolysis bullosa dystrophica, autosomal dominant [2] )
Dystrophic epidermolysis bullosa, autosomal recessive ( Epidermolysis bullosa dystrophica, autosomal recessive [14] )
Dystrophic epidermolysis bullosa, pretibial ( Epidermolysis bullosa dystrophica, pretibial [3] )
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Php programming by
Robert Barbey
Edited by Aldo Campana, November 3, 2009
