DiGeorge Syndrome |
Dysautonomia, Familial |
Deficiencies, Factor XI |
Dermal Hypoplasias, Focal |
Dariers Disease |
Disease, Wolman |
Dysostoses, Mandibulofacial |
Dorfman Chanarin syndrome |
Dystrophies, Vitelliform Macular |
Diabetes Insipidus, Neurogenic |
Denys Drash Syndrome |
Doyne honeycomb retinal dystrophy |
Diabetes Mellitus, Permanent Neonatal |
Dysplasias, Campomelic |
Deafness, Autosomal Dominant 9 |
Diarrhea 5, With Tufting Enteropathy, Congenital |
Deficiencies, Factor XIII |
Dystonia 6, torsion |
Dent disease 1 |
Deficiencies, Factor XII |
Deafness, Autosomal Recessive 9 |
Distal arthrogryposis type 2B |
Donnai-Barrow syndrome |
Deafness, Autosomal Recessive 12 |
Deafness, Autosomal Recessive 2 |
Deafness, Autosomal Dominant 13 |
Deafness, Autosomal Recessive 23 |
Deafness, Autosomal Recessive 48 |
Deafness, Autosomal Recessive 3 |
Deafness, Autosomal Dominant 36 |
Deafness, Autosomal Dominant 25 |
Dicarboxylicaminoaciduria |
Diabetes Insipidus, Nephrogenic |
Diastrophic dysplasia |
Dyskeratosis Congenita |
Dystrophies, Oculopharyngeal Muscular |
De Lange Syndrome |
Disease, Dent's |
Deafness, Autosomal Dominant 12 |
Deafness, Autosomal Recessive 7 |
Deafness, Autosomal Recessive 68 |
Diabetes Mellitus, Transient Neonatal, 2 |
Deafness, Autosomal Recessive 37 |
Deafness, Autosomal Recessive 59 |
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism |
Deafness, Autosomal Recessive 42 |
Deafness, Autosomal Recessive 63 |
Deafness, Autosomal Recessive 1A |
Deafness, autosomal dominant nonsyndromic sensorineural 22 |
Dyssegmental dysplasia |
Deafness, Autosomal Recessive 16 |
Deafness, Autosomal Recessive 30 |
Deafness, Autosomal Recessive 49 |
Deafness, Autosomal Recessive 79 |
Deficiencies, Factor X |
Disease, Gilbert |
Deficiencies, Protein C |
Dyschromatosis symmetrica hereditaria 1 |
Dystonia 3, Torsion, X-Linked |
Deafness, Autosomal Recessive 31 |
Deafness, Autosomal Recessive 22 |
Dystonia, Dopa-responsive |
Distal myopathy, Nonaka type |
Deafness, Autosomal Recessive 18 |
Dementia, familial British |
Dystonia 12 |
Deficiencies, Dihydropyrimidine Dehydrogenase |
Dmd-Associated Dilated Cardiomyopathy |
Dystonia musculorum deformans type 1 |
Desmosterolosis |
Deficiencies, Factor V |
Dyggve-Melchior-Clausen syndrome |
Deficiency, Prolidase |
Dystonia-Parkinsonism, Adult-Onset |
Diarrhea 3, Secretory Sodium, Congenital |
Dystonia 18 |
Deficiencies, Factor VII |
Deafness, Autosomal Dominant 11 |
Deafness, X-Linked 1 |
Deficiency of interleukin-1 receptor antagonist |
Dimauro disease |
Deafness, Autosomal Dominant 10 |
Diaphanospondylodysostosis |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia |
Deafness, Autosomal Recessive 4 |
Duane Retraction Syndrome |
Diseases, Pulmonary Veno-Occlusive |
Diabetes Mellitus, Transient Neonatal, 1 |
Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis |
Dyskinesia, Familial, with Facial Myokymia |
Dystonia musculorum deformans 4 |
Dystonia 16 |
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency |
dopamine beta hydroxylase deficiency |
Dihydropyrimidinase Deficiency |
Dentinogenesis imperfecta, shields type 3 |
Deafness, Autosomal Dominant 4 |
Digital Arthropathy-Brachydactyly, Familial |
Deafness, Autosomal Dominant 17 |
Deafness, Autosomal Recessive 53 |
Deafness, Autosomal Dominant 15 |
Diamond-Blackfan Anemia 10 |
Dwarfism, cortical thickening of tubular bones, and transient hypocalcemia |
Dentinogenesis Imperfecta |
Depressive Disorders |
Diabetes Insipidus |
Diabetes Mellitus |
Dystonia |
Disease, Hirschsprung |
Diseases, Kidney |
Disease, Machado-Joseph |
Deficiencies, alpha 1-Antitrypsin |
Degeneration, Macular |
De Barsy syndrome |
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans |
Dementia |
Digitorenocerebral Syndrome |
Disorder, Major Depressive |
Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8 |
Deafness, Autosomal Recessive 6 |
Deafness, Autosomal Dominant 6 |
Diarrhea 4, Malabsorptive, Congenital |
Deafness, Autosomal Recessive 32 |
Deafness, Autosomal Recessive 35 |
Diffuse palmoplantar keratoderma, Bothnian type |
Deafness, X-Linked 5 |
Dent Disease 2 |
Dystonia, juvenile-onset |
Dosage-sensitive sex reversal |
Diabetes Mellitus, Insulin-Dependent, 2 |
Deafness, Autosomal Recessive 67 |
Deafness, Autosomal Recessive 28 |
Dimethylglycine Dehydrogenase Deficiency |
Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1 |
Dystonia musculorum deformans type 2 |
Deafness, Autosomal Recessive 66 |
Deafness, Autosomal Dominant 20 |
Diabetes Mellitus, Transient Neonatal, 3 |
Deafness, Autosomal Recessive 15 |
Deafness, Autosomal Recessive, 24 |
Deafness, Autosomal Dominant 2B |
Deafness, Autosomal Dominant 3B |
Diamond-Blackfan Anemia 7 |
Dyschromatosis Universalis Hereditaria 1 |
Deafness, Autosomal Dominant 3A |
Diamond-Blackfan Anemia 5 |
Diabetes Mellitus, Insulin-Dependent, 20 |
Deafness, Autosomal Dominant 2A |
Diamond-Blackfan Anemia 9 |
Dystransthyretinemic Euthyroidal Hyperthyroxinemia |
Dowling-Degos Disease |
Diamond-Blackfan Anemia 1 |
Disabilities, Intellectual |
Dysplasias, Polyostotic Fibrous |
Dilated cardiomyopathy, familial |
Desmoid disease, hereditary |
Double Outlet Right Ventricle |
Dysfibrinogenemia, Congenital |
Dermatopathia pigmentosa reticularis |
Deafness, Autosomal Dominant 5 |
De La Chapelle Dysplasia |
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant |
Dwarfism |
Deficiencies, Riboflavin |
D-glycericacidemia |
Deafness, Autosomal Dominant 28 |
Deafness, X-Linked 4 |
Deafness, Autosomal Dominant 1 |
Deafness, Autosomal Recessive 77 |
Dehydration |
Depressions |
Diabetic Nephropathies |
Diabetic Retinopathies |
Dystrophy, Fuchs' Endothelial |
Diseases, Glycogen Storage |
Diseases, Lung |
Defect, Neural Tube |
Disorders, Obsessive-Compulsive |
Degeneration, Retinal |
Dysplasia, Thanatophoric |
Diabetes, Gestational |
Dystrophies, Facioscapulohumeral Muscular |
Dysfunction, Erectile |
De Sanctis-Cacchione syndrome |
Desmoplastic Small Round Cell Tumor |
Dysfunction, Cognitive |
Desbuquois syndrome |
Deafness, Autosomal Recessive 39 |
Deafness, Autosomal Dominant 41 |
Deafness, Autosomal Recessive 26 |
Deafness, Autosomal Dominant 23 |
Diaphragmatic Hernia 3 |
Deafness, Autosomal Recessive 44 |
Diaphyseal medullary stenosis with malignant fibrous histiocytoma |
Deafness, Autosomal Recessive 21 |
Deafness, Congenital Heart Defects, and Posterior Embryotoxon |
Deafness, Sensorineural, And Male Infertility |
Deafness, Digenic, Gjb2-Gjb6 |
Deafness, Digenic, Gjb2-Gjb3 |
Deafness, Autosomal Recessive 1b |
Diamond-Blackfan Anemia 8 |
Diamond-Blackfan Anemia 4 |
Demyelinating Disease |
Dysfunction, Left Ventricular |
Distal Myopathy |
Developmental Delay, Epilepsy, and Neonatal Diabetes |
Diseases, Heart |
Disease, Hodgkin |
Disorder, Iron Metabolism |
Deafness enamel hypoplasia nail defects |
Deoxyguanosine Kinase Deficiency |
Dandy Walker Syndrome |
Diabetic Neuropathies |
Disorder, Lymphoproliferative |
Diabetic Cardiomyopathy |
Diaphragmatic Hernias |
Disease, Hyaline Membrane |
Dentin dysplasia, type 1 |
Deafness, Autosomal Dominant 44 |
Deafness |
Diabetes Mellitus, Experimental |
Ductus Arteriosus, Patent |
Drug-Induced Dyskinesia |
Diseases, Eye |
Disease, Hereditary Eye |
Disease, Graves' |
Disease, Heart Valve |
Dystrophies, Muscular |
Disorder, Myeloproliferative |
Degeneration, Nerve |
Disorder, Psychotic |
Detachment, Retinal |
Disease, Retinal |
de Pointes, Torsade |
Drug-Related Side Effects and Adverse Reactions |
Diseases, Vascular |
Dysraphism, Spinal |
Disorder, Migraine |
Dysprothrombinemia |
Dyslexia |
Dystrophy, Retinal |
Diabetes Mellitus, Noninsulin-Dependent, 1 |
Deafness, Aminoglycoside-Induced |
Dermodistortive Urticaria |
Deafness, Sensorineural, Autosomal-Mitochondrial Type |
Dysgnathia complex |
Deficiencies, Glucosephosphate Dehydrogenase |
Duodenal Ulcer |
Deglutition Disorders |
Dwarfism, Pituitary |
Diarrhea |
Defect, Congenital Heart |
Dyserythropoietic Anemia with Thrombocytopenia |
Diverticulitides |
Defect, Heart Septal |
Developmental Disabilities |
Diabetic Ketoacidoses |
Dyssomnias |
Dursun Syndrome |
Diverticular Diseases |
Disorders, Mental |
Death, Sudden |
Delirium |
Dengue |
Dermatitides |
Dermatomyositides |
Dextrocardia |
Down Syndrome |
Dysarthria |
Dyskinesia |
Dystonia Musculorum Deformans |
Disease, Graft-vs-Host |
Diseases, Liver |
Disease, Metabolic |
Diseases, Nervous System |
Disorders, Panic |
Disease, Skin |
Disorder, Temporomandibular Joint |
Disease, Thyroid |
Deficiencies, Vitamin D |
Deficiencies, Vitamin E |
Dermatofibrosarcoma |
Dyslipidemia |
Deficiencies, Protein S |
Delta-Beta Thalassemia |
Diabetes Complications |
Dystonic Disorder |
Degenerations, Frontotemporal Lobar |
Ductal Carcinoma |
Dysgenesis, Thyroid |
Deafness, Autosomal Recessive |
Doughnut Lesions of Skull, Familial |
Dermatitis, Atopic, 2 |
Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant |
Distal Hereditary Motor Neuropathy, Type II |
Dyskeratosis Congenita, Autosomal Dominant |
Dysequilibrium syndrome |
Disorders, Paranoid |
Diffuse Cerebral Sclerosis of Schilder |
Disease, Virus |
Dermatitis, Allergic Contact |
Depression, Postpartum |
Disease, Periodontal |
Dystrophy, Neuroaxonal |
Dysosteosclerosis |
Drug Eruptions |
Dyspnea |
Diseases of Endocrine System |
Disruptive, Impulse Control, and Conduct Disorders |
Disease, Intestinal |
Disease, Legionnaire |
Diseases, Respiratory Tract |
Degeneration, Spinocerebellar |
Deficiencies, Vitamin A |
Dysfunction, Right Ventricular |
Diffuse Scleroderma |
Diabetes Mellitus, Lipoatrophic |
Dry Eye Syndromes |
Dysthymic Disorder |
Dysplasias, Monostotic Fibrous |
Diseases, Gastrointestinal |
Disease, Hematologic |
Development Disorder, Language |
Disease, Meniere |
Disease, Pleural |
Disorder, Shared Paranoid |
Disease, Testicular |
Dubowitz syndrome |
Dysfunction, Ventricular |
Disorder, Pigmentation |
Disorder, Myotonic |
Diabetes Mellitus, Insulin-Dependent, 12 |
Dystonia, Primary Cervical |
Dyskeratosis Congenita, Autosomal Recessive |
Dementia, Vascular |
Dental Enamel Hypoplasia |
Digestive System Neoplasm |
Drug Hypersensitivities |
Dysgammaglobulinemia |
Dysmenorrhea |
Dysostoses |
Disease, Ear |
Disease, Esophageal |
Diseases, Eyelid |
Dermatoses, Facial |
Disease, Fetal |
Deformities, Foot |
Disease, Male Genital |
Disorder, Growth |
Deformities, Hand |
Disorder, Hemorrhagic |
Disease, Hepatic Veno-Occlusive |
Delayed Hypersensitivities |
Diseases of Immune System |
Disc Displacement, Intervertebral |
Duct Obstruction, Lacrimal |
Diseases, Lens |
Disease, Parasitic Liver |
Deficiencies, Magnesium |
Disease, Mandibular |
Disease, Maxillary |
Diseases, Mouth |
Diseases, Nail |
Disorder, Opioid-Related |
Dermatitides, Occupational |
Disease, Occupational |
Disease, Ovarian |
Drug Overdose |
Disease, Pancreatic |
Disease, Penile |
Diseases, Pituitary |
Disease, Placenta |
Disease, Prostatic |
Deficiencies, Protein |
Dysfunction, Psychological Sexual |
Disorder, Puerperal |
Disorders, Respiration |
Dysplasia, Retinal |
Deprivation, Sleep |
Disease, Splenic |
Disease, Stomach |
Disease, Stomatognathic |
Deficiencies, Thiamine |
Disease, Thoracic |
Diseases, Tooth |
Disorder, Urination |
Disease, Uterine |
Disease, Vestibular |
Degeneration, Wallerian |
Disease, Peripheral Vascular |
Dermatitis, Irritant |
Dermatitis, Photoallergic |
Deficiency Syndrome, Leukocyte Adhesion |
Degeneration, Striatonigral |
Disorder, Heat Stress |
Disorder, Phobic |
Delayed Emergence from Anesthesia |
Death, Infant |
Drinking, Binge |
Deafness, congenital onychodystrophy, recessive form |
DNA Repair Deficiency Disorders |
Diabetes Mellitus, Permanent Neonatal, With Neurologic Features |
Drug Metabolism, Poor, CYP2C19-Related |
Drug Metabolism, Poor, CYP2D6-Related |
Deafness, Autosomal Dominant 48 |
Dystonia 13, Torsion |
Dwarfism tall vertebrae |
Drusen, Radial, Autosomal Dominant |
Digitotalar Dysmorphism |
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema |
Duplication 15q11-q13 Syndrome |
Desmoid Tumor Caused By Somatic Mutation |
Diabetes Mellitus, Insulin-Dependent, 22 |
Dystonia 17, Torsion, Autosomal Recessive |
Deafness, autosomal dominant nonsyndromic sensorineural 17 |
Deletion 11p13 |
Disorder, Sleep Wake |
Disease, Lysosomal Storage |
Decompression Sickness |
Dementia, Multi Infarct |
Dental Pulp Exposure |
Dentin Dysplasia |
Dilatation, Pathologic |
Dysentery |
Dyspepsia |
Disease, Hemoglobin SC |
Diseases, Lymphatic |
Disease, Periapical |
Deficiencies, Potassium |
Degeneration, Retrograde |
Disease, Rheumatic Heart |
Diseases, Spinal |
Disease, Submandibular Gland |
Deficiencies, Vitamin B |
Disease, Weil |
Degenerative Myopias |
Disease, Pelvic Inflammatory |
Diabetes Mellitus, Insulin-Dependent, 7 |
Dysferlinopathy |
Dysbiosis |
Dysphonia |
Delusion |
Dental Caries |
Dissecans, Osteochondritis |
delta-Thalassemias |
Darier Disease, Segmental |
Disgerminomas |
Dermatitis, Exfoliative |
Diaphragmatic Eventration |
Distensae, Striae |
Duodenal atresia |
Dacryocystitides |
Decerebrate State |
Diagnostic Techniques, Cardiovascular |
Diastema |
Digestive System Disease |
Diphtheria |
Diplopia |
Dyspnea, Paroxysmal |
Dysuria |
Diverticulum, Esophageal |
Dysplasias, Fibromuscular |
Disease, Ileal |
Disease, Laryngeal |
Diverticulum, Meckel |
Disorders, Neurotic |
Disease, Orbital |
Diseases, Rheumatic |
Dermatitis, Seborrheic |
Disease, Infectious Skin |
Diabetic Foot |
Duodenal stenosis |
Digestive System Abnormalities |
Dyskinesias, Tardive |
Dyscalculias |
Disomies, Uniparental |
Dyspareunia |
Darier Disease, Acral Hemorrhagic Type |
Deafness, Autosomal Dominant 16 |
Down Syndrome Critical Region |
Deafness, nonsyndromic sensorineural, mitochondrial |
Deafness, Sensorineural, with Hypertrophic Cardiomyopathy |
Degeneration, Paraneoplastic Cerebellar |
Dilution, Pigmentary |
Disease, Parasitic |
Dysplastic Nevus Syndrome |
Disease, Sexually Transmitted |
Disease, Tracheal |
Dermatitis Herpetiformis |
Diseases, Parathyroid |
Deficiencies, Vitamin K |
Dipsogenic Diabetes Insipidus |
Dyschromatosis universalis hereditaria |
Disease, Foot-and-Mouth |
Disorders, Schizotypal Personality |
Dermatitis, Phototoxic |
Distemper |
Disease, Paranasal Sinus |
Dysphoric Disorder, Premenstrual |
Double cortex |
Discitides |
Diseases, Gallbladder |
Deficiency Disease, Mannosidase |
Dentin Sensitivities |
Dizziness |
Dumping Syndrome |
Duodenitis |
Diseases, Female Genital |
Disease, Iatrogenic |
Disease, Whipple |
Disorganized Schizophrenia |
Denture Stomatitides |
Disease, Urologic |
Discharge, Nipple |
De Quervain Disease |
Dysplasia epiphysealis hemimelica |
Dendritic Cell Sarcoma, Follicular |
Dendritic Cell Sarcoma, Interdigitating |
Diabetes Mellitus, Noninsulin-Dependent, 2 |
Deafness, Autosomal Recessive 10 |
Dystonia, Focal, Task-Specific |
Dianzani autoimmune lymphoproliferative syndrome |
Dental Calculus |
Dental Plaque |
Dental Pulp Diseases |
Dental Pulp Necroses |
Dentin, Secondary |
Dependent Personality Disorder |
Depersonalization |
Dermatomycoses |
Dermatosis Papulosa Nigra |
Diarrhea, Infantile |
Dictyocaulus Infection |
Dirofilariases |
Disorders, Dissociative |
Diverticulitis, Colonic |
Diverticulum |
Disease, Duodenal |
Duodenal Neoplasm |
Deformities, Equinus |
Disorder, Esophageal Motility |
Diffuse Esophageal Spasm |
Diseases, Facial Nerve |
Disease, Gingival |
Disease, Heartwater |
Disorder, Malignant Histiocytic |
Disorders of Excessive Somnolence |
Disorder, Immunoproliferative |
Disease, Parasitic Intestinal |
Diseases, Iris |
Disease, Lumpy Skin |
Disease, Mikulicz |
Disease, Nasopharyngeal |
Diseases, Nose |
Disease, Otorhinolaryngologic |
Disorder, Photosensitivity |
Dystrophies, Reflex Sympathetic |
Disease, Salivary Gland |
Disorder, Schizoid Personality |
Disease, Parasitic Skin |
Diseases, Tongue |
Disease, Vaginal |
Detachment, Vitreous |
Disease, Vulvar |
Digestive System Fistula |
Dandruff |
Dermatitides, Perioral |
Diastases, Bone |
Diffuse alopecia |
Dyssegmental dysplasia, Rolland-Desbuquois type |
Deciduoma |
Dysentery, Bacillary |
Delayed Graft Function |
Digeorge Syndrome-Velocardiofacial Syndrome Complex 2 |
Dermatitis herpetiformis, familial |
Diabetes Mellitus, Insulin-Dependent, 8 |
Dermoids of cornea |
Deafness-Hypogonadism Syndrome |
Deafness, Autosomal Recessive 17 |
Deaf-Blind Disorder |
Dystonia with Cerebellar Atrophy |
Dyschromatosis Universalis Hereditaria 2 |
Dandy Walker variant |
Desmoplastic cerebral astrocytoma of infancy |
Distal Trisomy 10q Syndrome |
Dandy Walker cyst |
Dermatitides, Digital |
Disorder, Pelvic Floor |
Dentofacial Deformities |
Disorder, Specific Learning |
Deficiency Disease |
Dental Health Service |
Dermis |
Diencephalon |
Diffusion |
Diseases |
Disease Susceptibilities |
Dislocations, Joint |
Duplication, Gene |
Duct, Nasolacrimal |
Disk, Optic |
Discharge, Patient |
Development, Psychosexual |
Diaphyses |
Disorder, Late Onset |
Drinking Water |
Development, Muscle |
Dystonia 15, myoclonic |