Clinical Trials Involving Rare Diseases: H
- HELLP Syndrome (26)
- HIVEP2-related Intellectual Disability (1)
- HTLV-1 Associated Myelopathy/tropical Spastic Paraparesis (11)
- Haemophilus Influenzae (200)
- Hailey-Hailey Disease (4)
- Hairy Cell Leukemia (224)
- Hansen's Disease (34)
- Hantavirus Pulmonary Syndrome (14)
- Hashimoto Encephalopathy (25)
- Heart Tumor (10)
- Heavy Metal Poisoning (44)
- Helminthiasis (286)
- Hemangioblastoma (13)
- Hemangioendothelioma (22)
- Hemangioma Thrombocytopenia Syndrome (7)
- Hemangiopericytoma (60)
- Hemicrania Continua (3)
- Hemifacial Microsomia (6)
- Hemihypertrophy (2)
- Hemimegalencephaly (2)
- Hemochromatosis Type 3 (50)
- Hemochromatosis Type 4 (1)
- Hemoglobin C Disease (7)
- Hemoglobin SC Disease (32)
- Hemolytic Uremic Syndrome (50)
- Hemophilia (706)
- Hemophilia A (682)
- Hemophilia B (208)
- Hemophilic Arthropathy (26)
- Hemosiderosis (28)
- Henoch-Schonlein Purpura (26)
- Heparin-induced Thrombocytopenia (42)
- Hepatic Encephalopathy (169)
- Hepatic Veno-occlusive Disease (20)
- Hepatitis D (48)
- Hepatitis E (29)
- Hepatoblastoma (64)
- Hepatopulmonary Syndrome (12)
- Hepatorenal Syndrome (43)
- Hereditary Amyloidosis (9)
- Hereditary Angioedema (114)
- Hereditary Antithrombin Deficiency (14)
- Hereditary Antithrombin Deficiency Type 2 (1)
- Hereditary Ataxia (7)
- Hereditary Cerebral Hemorrhage With Amyloidosis (17)
- Hereditary Coproporphyria (12)
- Hereditary Diffuse Gastric Cancer (7)
- Hereditary Diffuse Leukoencephalopathy With Spheroids (3)
- Hereditary Elliptocytosis (1)
- Hereditary Fructose Intolerance (9)
- Hereditary Hemorrhagic Telangiectasia (72)
- Hereditary Leiomyomatosis and Renal Cell Cancer (8)
- Hereditary Melanoma (2)
- Hereditary Methemoglobinemia (1)
- Hereditary Motor and Sensory Neuropathy (432)
- Hereditary Multiple Osteochondromas (5)
- Hereditary Neuropathy With Liability to Pressure Palsies (432)
- Hereditary Pancreatitis (9)
- Hereditary Paraganglioma-pheochromocytoma (1)
- Hereditary Sensory Neuropathy Type 1 (1)
- Hereditary Sensory and Autonomic Neuropathy (15)
- Hereditary Spastic Paraplegia (21)
- Hereditary Spherocytosis (5)
- Hermansky-Pudlak Syndrome (10)
- Herpes Simiae (B Virus) (408)
- Herpes Simplex Encephalitis (3)
- Herpes Zoster Ophthalmicus (2)
- Herpes Zoster Oticus (1)
- Heterotaxy (6)
- Hidradenocarcinoma (1)
- Hirschsprung Disease (45)
- His Bundle Tachycardia (1)
- Hodgkin Lymphoma (1,327)
- Holoprosencephaly (5)
- Homocystinuria (10)
- Homocystinuria Due to CBS Deficiency (3)
- Homologous Wasting Disease (862)
- Horizontal Gaze Palsy With Progressive Scoliosis (2)
- Horner's Syndrome (6)
- Hoyeraal Hreidarsson Syndrome (1)
- Human HOXA1 Syndromes (1)
- Human T-cell Leukemia Virus Type 1 (51)
- Human T-cell Leukemia Virus Type 2 (6)
- Huntington Disease (205)
- Hurler Syndrome (58)
- Hurler–Scheie Syndrome (17)
- Hurthle Cell Thyroid Cancer (6)
- Hyaline Fibromatosis Syndrome (1)
- Hydatidiform Mole (13)
- Hydatidosis (17)
- Hydrops Fetalis (8)
- Hyper IgE Syndrome (12)
- Hyper-IgD Syndrome (3)
- Hyperacusis (16)
- Hyperadrenalism (215)
- Hypereosinophilic Syndrome (133)
- Hyperinsulinism-hyperammonemia Syndrome (2)
- Hyperkalemic Periodic Paralysis (2)
- Hyperlipidemia Type 3 (5)
- Hyperlipoproteinemia Type 4 (1)
- Hyperlipoproteinemia Type 5 (10)
- Hypermobile Ehlers-Danlos Syndrome (7)
- Hyperprolinemia (1)
- Hypersensitivity Pneumonitis (22)
- Hypersensitivity Vasculitis (2)
- Hypoaldosteronism (8)
- Hypochondroplasia (4)
- Hypocomplementemic Urticarial Vasculitis (7)
- Hypoganglionosis (3)
- Hypohidrotic Ectodermal Dysplasia (19)
- Hypokalemic Periodic Paralysis (3)
- Hypolipoproteinemia (25)
- Hypomelanotic Disorder (195)
- Hypoparathyroidism (113)
- Hypopharyngeal Cancer (368)
- Hypophosphatasia (32)
- Hypophosphatemic Rickets (55)
- Hypopituitarism (171)
- Hypoplastic Left Heart Syndrome (60)
- Hypoplastic Right Heart Syndrome (3)
- Hypothalamic Obesity (12)
- Hypotrichosis Simplex (1)
- Hypoxanthine Guanine Phosphoribosyltransferase Deficiency (4)