Find Technology Related to a Rare Disease

Click on a letter to view the rare diseases.

 

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

A

Acne Rosacea
Acoustic Neuroma
Acquired Aplastic Anemia
Acromesomelic Dysplasia
Acromicric Dysplasia
ACTH Deficiency
Acute Respiratory Distress Syndrome
Adams Oliver Syndrome
Addison's Disease
Adenoid Cystic Carcinoma
Adenylosuccinate Lyase Deficiency
Adrenal Hyperplasia, Congenital (General)
Adult Onset Still's Disease
Adult Panic Anxiety Syndrome
Agenesis of Corpus Callosum
Agnosia, Primary Visual
Agranulocytosis, Acquired
AIDS (Acquired Immune Deficiency Syndrome)
AIDS Dysmorphic Syndrome
Albinism, Ocular
Alexander Disease
Alopecia Areata

B

Barrett Esophagus
Barth Syndrome
Beals Syndrome
Beckwith Wiedemann Syndrome
Bell's Palsy
Benign Essential Tremor
Bernard Soulier Syndrome
Best Vitelliform Macular Dystrophy
Binswanger's Disease
Biotinidase deficiency
Birt-Hogg-Dube Syndrome
Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex
Blepharospasm, Benign Essential
Bloom Syndrome
Blue Diaper Syndrome
Blue Rubber Bleb Nevus Syndrome
Botulism
Bowen Hutterite Syndrome
Brachial Plexus Palsy
Brain Tumors, General
Branchio Oculo Facial Syndrome
Branchio Oto Renal Syndrome
Bronchiolitis Obliterans Organizing Pneumonia
Bronchopulmonary Dysplasia (BPD)
Brown Sequard Syndrome
Brown Syndrome
Brugada Syndrome

C

CADASIL
Canavan Disease
Cancer, Colon
Cancer, Prostate
Cancers, Skin, General
Carbamyl Phosphate Synthetase Deficiency
Carcinoid syndrome
Carcinoma, Renal Cell
Carcinoma, Squamous Cell
Carney Complex
Carnitine Palmitoyltransferase 1A Deficiency
Carpal Tunnel Syndrome
Castleman's Disease
Cat Eye Syndrome
Caudal Regression Syndrome
Cavernous Malformation
Central Core Disease
Central Diabetes Insipidus
Central Hypoventilation Syndrome, Congenital
Cerebellar Degeneration, Subacute
Cerebral Palsy
Cerebro Oculo Facio Skeletal Syndrome
Cervical Dystonia
Cervical Teratoma
Chagas Disease
Charcot Marie Tooth Disease
CHARGE Syndrome

D

Dandy Walker Malformation
De Barsy Syndrome
Dengue Fever
Dense Deposit Disease
Dentin Dysplasia, Type I
Dentin Dysplasia Type II
Dentinogenesis Imperfecta Type III
Dermatitis, Atopic
Dermatitis, Contact
Dermatitis Herpetiformis
De Santis Cacchione Syndrome
Desmoid Tumor
Diabetes, Insulin Dependent
Diastrophic Dysplasia
Diffuse Idiopathic Skeletal Hyperostosis
Dilatation of the Pulmonary Artery, Idiopathic
Distal Myopathy
DOOR Syndrome
Down Syndrome
Dubin Johnson Syndrome
Duodenal Atresia or Stenosis
Dysautonomia, Familial
Dysplasia Epiphysealis Hemimelica
Dysplasia, Fibrous
Dystonia
Dystrophy, Asphyxiating Thoracic
Dystrophy, Myotonic

E

Ear, Patella, Short Stature Syndrome
Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate
Edema, Idiopathic
Ellis Van Creveld Syndrome
Emphysema, Congenital Lobar
Encephalitis, Herpes Simplex
Encephalitis, Japanese
Encephalitis, Rasmussen's
Endocarditis, Infective
Endometriosis
Endomyocardial Fibrosis
Epidermal Nevus Syndrome
Epitheliopathy, Acute Posterior Multifocal Placoid Pigment
Erythrokeratodermia with Ataxia
Esophageal Atresia and/or Tracheoesophageal Fistula
Essential Iris Atrophy
Ewing's Sarcoma

F

Fabry Disease
Facioscapulohumeral Muscular Dystrophy
Factor XIII Deficiency
Familial Adenomatous Polyposis
Familial Cold Autoinflammatory Syndrome
Familial Encephalopathy with Neuroserpin Inclusion Bodies
Familial Eosinophilic Cellulitis
Familial Hypercholesterolemia
Familial Idiopathic Basal Ganglia Calcification
Familial Juvenile Hyperuricemic Nephropathy
Familial Lipoprotein Lipase Deficiency
Femoral Facial Syndrome
Fetal Alcohol Syndrome
Fetal Hydantoin Syndrome
Fetal Retinoid Syndrome
Fetal Valproate Syndrome
FG Syndrome Type 1
Fiber Type Disproportion, Congenital
Fibrodysplasia Ossificans Progressiva (FOP)
Fibromatosis, Congenital Generalized
Fibromuscular Dysplasia
Floating Harbor Syndrome
Focal Dermal Hypoplasia
Formaldehyde Poisoning
Fox Fordyce Disease
Fragile X Syndrome
Fraser Syndrome
Freeman Sheldon Syndrome
Free Sialic Acid Storage Disorders
Frontofacionasal Dysplasia
Frontonasal Dysplasia
Fructose Intolerance, Hereditary
Fukuyama Type Congenital Muscular Dystrophy

G

Galactosemia
Gastritis, Chronic, Erosive
Gastritis, Giant Hypertrophic
Gastroesophageal Reflux
Gastrointestinal Stromal Tumors
Gaucher Disease
Giant Axonal Neuropathy
Giant Cell Myocarditis
Gilbert Syndrome
Glioblastoma Multiforme
Glucose-6-Phosphate Dehydrogenase Deficiency
Glutaricaciduria II
Glycogen Storage Disease Type I
Glycogen Storage Disease Type V
Glycogen Storage Disease Type VII
Glycogen Storage Disease VIII
Goodman Syndrome
Gordon Syndrome
Graft versus Host Disease
Granulomatous Disease, Chronic
Graves' Disease
Growth Delay, Constitutional
Growth Hormone Deficiency
Guillain Barré Syndrome

H

Hageman Factor Deficiency
Hantavirus Pulmonary Syndrome
Headache, Cluster
Heart Block, Congenital
Heavy Metal Poisoning
Hematuria, Benign, Familial
Hemochromatosis, Classic Hereditary
Hemophilia
Hemophilia B
Hemorrhagic Telangiectasia, Hereditary
Henoch-Schonlein Purpura
Hepatic Encephalopathy
Hepatic Fibrosis, Congenital
Hepatitis B
Hepatitis C
Hepatitis, Neonatal, Idiopathic
Hereditary Exostoses, Multiple
Hereditary Hyperphosphatasia
Hermansky Pudlak Syndrome
Herpes, Neonatal
Hiccups, Chronic
Hodgkin's Disease
Homocystinuria due to Cystathionine Beta-Synthase Deficiency
HTLV Type I and Type II
Human Granulocytic Ehrlichiosis (HGE)
Human HOXA1 Syndromes
Human Monocytic Ehrlichiosis (HME)
Huntington's Disease
Hydrocephalus

I

I Cell Disease
Ichthyosis
Ichthyosis, Chanarin Dorfman Syndrome
Ichthyosis, CHILD Syndrome
Ichthyosis, Erythrokeratodermia Variabilis
Ichthyosis, Erythrokeratolysis Hiemalis
Ichthyosis, Harlequin Type
Ichthyosis Hystrix, Curth Macklin Type
Ichthyosis, Keratosis Follicularis Spinulosa Decalvans
Ichthyosis, Lamellar
Ichthyosis, Netherton Syndrome
Ichthyosis, Sjogren Larsson Syndrome
Ichthyosis, Trichothiodystrophy
Ichthyosis Vulgaris
Ichthyosis, X Linked
Idiopathic Pulmonary Fibrosis
Idiopathic Thrombocytopenic Purpura
IgA Nephropathy
Infantile Neuroaxonal Dystrophy
Interstitial Cystitis
Intestinal Pseudoobstruction
Irritable Bowel Syndrome

J

Jansen Type Metaphyseal Chondrodysplasia
Joubert Syndrome
Juvenile Hemochromatosis
Juvenile Pilocytic Astrocytoma

K

Kasabach-Merritt phenomenon
Kawasaki Disease
Kennedy Disease
Keratitis Ichthyosis Deafness Syndrome
Keratosis, Seborrheic
Klinefelter Syndrome
Kniest Dysplasia

L

L1 Syndrome
LADD Syndrome
Landau Kleffner Syndrome
Langerhans Cell Histiocytosis
Larsen Syndrome
Leber Congenital Amaurosis
Leber Hereditary Optic Neuropathy
Lenz Microphthalmia Syndrome
Leprosy
Leukemia, Chronic Lymphocytic
Leukemia, Chronic Myelogenous
Leukemia, Hairy Cell
Leukocyte Adhesion Deficiency Syndromes
Leukodystrophy, Krabbe's
Locked In Syndrome
Loken Senior Syndrome
Lowe Syndrome
Low Gamma-GT Familial Intrahepatic Cholestasis
Lupus
Lyme Disease
Lymphatic Malformations
Lymphedema, Hereditary
Lymphocytic Infiltrate of Jessner
Lymphoma, Gastric, Non Hodgkins Type

M

Machado-Joseph Disease
Macular Degeneration
Malaria
Mal de Debarquement
Malignant Hyperthermia
Mallory Weiss Syndrome
Manic Depression, Bipolar
Mantle Cell Lymphoma
Maple Syrup Urine Disease
Marcus Gunn Phenomenon
Marden Walker Syndrome
Marshall Smith Syndrome
Marshall Syndrome
Mastocytosis
Maxillonasal Dysplasia, Binder Type
May Hegglin Anomaly
MCT8-specific thyroid hormone cell transporter deficiency
Measles
Mediterranean Fever, Familial
Medium Chain Acyl CoA Dehydrogenase Deficiency
Medullary Sponge Kidney
Megalocornea Mental Retardation Syndrome
Melanoma, Malignant
Melkersson Rosenthal Syndrome
Melnick Needles Syndrome
Meningitis, Bacterial
Menkes Disease

N

N-Acetylglutamate Synthetase Deficiency
Nelson Syndrome
Neonatal Hemochromatosis
Neonatal Lupus
Neonatal-onset Multisystem Inflammatory Disease
Nephrogenic Diabetes Insipidus
Neu Laxova Syndrome
Neurodegeneration with Brain Iron Accumulation Type 1
Neurofibromatosis Type 1 (NF1)
Neurofibromatosis Type 2 (NF2)
Neuroleptic Malignant Syndrome
Neuropathy, Ataxia and Retinitis Pigmentosa
Neuropathy, Congenital Hypomyelination
Neuropathy, Hereditary Sensory, Type I
Neuropathy, Hereditary Sensory, Type II
Neuropathy, Hereditary Sensory, Type IV
Neuropathy, Peripheral
Neutropenia, Cyclic
Nevoid Basal Cell Carcinoma Syndrome
Niemann Pick Disease
Nystagmus, Benign Paroxysmal Positional

O

P

Q

Q Fever

R

Rabies
Radiation Syndromes
Ramsay Hunt Syndrome
Rapid-onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation
Rapp Hodgkin Syndrome
Raynaud's Disease and Phenomenon
Recurrent Respiratory Papillomatosis
Reflex Sympathetic Dystrophy Syndrome
Refractory Sprue
Relapsing Polychondritis
Renal Agenesis, Bilateral
Renal Glycosuria
Respiratory Distress Syndrome, Infant
Retinitis Pigmentosa
Retinoblastoma
Retinopathy, Arteriosclerotic
Retinopathy, Diabetic
Retinopathy, Hypertensive
Retinopathy of Prematurity
Retroperitoneal Fibrosis
Rett Syndrome
Rh Disease
Rheumatic Fever
Rickets, Vitamin D Deficiency
Ring Chromosome 4
Roberts Syndrome
Rocky Mountain Spotted Fever
Romano Ward Syndrome
Rosenberg Chutorian Syndrome
Rothmund Thomson Syndrome
Roussy Levy Syndrome
Russell Silver Syndrome (RSS)

S

Sacrococcygeal Teratoma
Sarcoidosis
Schimke Immuno-osseous Dysplasia
Schindler Disease
Schwartz Jampel Syndrome
Scleroderma
Scott Craniodigital Syndrome
Sennetsu Fever
Severe Combined Immunodeficiency
Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD)
SHORT Syndrome
Shwachman Syndrome
Sickle Cell Disease
Simian B Virus Infection
Simpson Dysmorphia Syndrome
Sinonasal Undifferentiated Carcinoma
Sirenomelia Sequence
Smallpox
Smith Lemli Opitz Syndrome
Smith Magenis Syndrome
Sneddon Syndrome
Spasmodic Dysphonia
Spinal Muscular Atrophy
Spinocerebellar Ataxia with Axonal Neuropathy
Split Hand/Split Foot Malformation
Spondyloepiphyseal Dysplasia, Congenital
Spondyloepiphyseal Dysplasia Tarda
Sporadic Inclusion Body Myositis
Sporadic Porencephaly
Status Epilepticus
Stenosis, Spinal

T

Tangier Disease
Tarsal Tunnel Syndrome
Tay Sachs Disease
Temporomandibular Joint Dysfunction (TMJ)
Tethered Cord Syndrome
Tetrahydrobiopterin Deficiency
Thalassemia Major
Thalassemia Minor
Thoracic Outlet Syndrome
Three M Syndrome
Thrombocythemia, Essential
Thrombocytopenia Absent Radius Syndrome
Thrombocytopenia, Essential
Thrombotic Thrombocytopenic Purpura
Thyroid Cancer
Timothy Syndrome
Tolosa Hunt Syndrome
Tongue Cancer
Tongue, Fissured
Tongue, Geographic
Tongue, Hairy
Tooth and Nail Syndrome
Tourette Syndrome
Toxic Epidermal Necrolysis
Toxic Shock Syndrome
Transverse Myelitis
Treacher Collins Syndrome
Trichorhinophalangeal Syndrome Type II
Trichorhinophalangeal Syndrome Type III
Trigeminal Neuralgia (Tic Douloureux)
Triosephosphate Isomerase Deficiency
Trisomy 13 Syndrome
Trisomy 18 Syndrome

U

Urticaria, Cholinergic
Urticaria, Cold
Urticaria, Physical
Urticaria Pigmentosa
Usher Syndrome
Uterine Leiomyosarcoma

V

VACTERL Association
VACTERL with Hydrocephalus
Varicella Zoster
Vascular Malformations of the Brain
Vasculitis, Cutaneous
Ventricular Septal Defects
Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)
Vitamin B12 Deficiency
Vitiligo
Von Hippel-Lindau Syndrome
Von Willebrand Disease

W

WAGR Syndrome/11p Deletion Syndrome
Walker Warburg Syndrome
Wandering Spleen
WAS Related Disorders
Weaver Syndrome
Werner Syndrome
West Nile Encephalitis
West Syndrome
Williams Syndrome
Wilms' Tumor
Wolff Parkinson White Syndrome
Wolf Hirschhorn Syndrome
Wyburn Mason Syndrome

X

X linked Juvenile Retinoschisis
X linked Lymphoproliferative Syndrome
X-Linked Myopathy with Excessive Autophagy
X-linked Opitz G/BBB syndrome

Y

Yellow Fever
Yellow Nail Syndrome

Z

Zellweger Spectrum Disorders