Filtering
- Gliomatosis Cerebri
- Gliosarcoma
- Glomerulonephritis
- Glossodynia
- Glossopharyngeal Neuralgia
- Glucagonoma
- Glucocorticoid Resistance
- Glucose-6-phosphate Dehydrogenase Deficiency
- Glucose-galactose Malabsorption
- Glucose Transporter Type 1 Deficiency Syndrome
- Glutaric Acidemia Type II
- Glutathione Synthetase Deficiency
- Glycogen Storage Disease Type 1A
- Glycogen Storage Disease Type 2
- Glycogen Storage Disease Type 3
- Glycogen Storage Disease Type 4
- Glycogen Storage Disease Type 5
- Glycogen Storage Disease Type 7
- GM1 Gangliosidosis
- GM3 Synthase Deficiency
- Goldenhar Disease
- Goldmann-Favre Syndrome
- Gonadal Dysgenesis
- Gonococcal Conjunctivitis
- Goodpasture Syndrome
- Gordon Syndrome
- Gorham's Disease
- Granular Cell Tumor
- Granulocytopenia
- Granuloma Annulare
- Granulomatosis With Polyangiitis
- Granulomatous Lobular Mastitis
- Granulomatous Slack Skin Disease
- Granulosa Cell Tumor of the Ovary
- Gray Platelet Syndrome
- Gray Zone Lymphoma
- Greig Cephalopolysyndactyly Syndrome
- Griscelli Syndrome
- Growth Hormone Deficiency
- GTP Cyclohydrolase I Deficiency
- Guillain-Barre Syndrome
- Guttate Psoriasis
- Gynandroblastoma
- Gyrate Atrophy of Choroid and Retina
- Haemophilus Influenzae
- Hailey-Hailey Disease
- Hairy Cell Leukemia
- Hansen's Disease
- Hantavirus Pulmonary Syndrome
- Hashimoto Encephalopathy
- Heart Tumor
- Heavy Metal Poisoning
- HELLP Syndrome
- Helminthiasis
- Hemangioblastoma
- Hemangioendothelioma
- Hemangioma Thrombocytopenia Syndrome
- Hemangiopericytoma
- Hemicrania Continua
- Hemifacial Microsomia
- Hemihypertrophy
- Hemimegalencephaly
- Hemochromatosis Type 3
- Hemochromatosis Type 4
- Hemoglobin C Disease
- Hemoglobin SC Disease
- Hemolytic Uremic Syndrome
- Hemophilia
- Hemophilia A
- Hemophilia B
- Hemophilic Arthropathy
- Hemosiderosis
- Henoch-Schonlein Purpura
- Heparin-induced Thrombocytopenia
- Hepatic Encephalopathy
- Hepatic Veno-occlusive Disease
- Hepatitis D
- Hepatitis E
- Hepatoblastoma
- Hepatopulmonary Syndrome
- Hepatorenal Syndrome
- Hereditary Amyloidosis
- Hereditary Angioedema
- Hereditary Antithrombin Deficiency
- Hereditary Antithrombin Deficiency Type 2
- Hereditary Ataxia
- Hereditary Cerebral Hemorrhage With Amyloidosis
- Hereditary Coproporphyria
- Hereditary Diffuse Gastric Cancer
- Hereditary Diffuse Leukoencephalopathy With Spheroids
- Hereditary Elliptocytosis
- Hereditary Fructose Intolerance
- Hereditary Hemorrhagic Telangiectasia
- Hereditary Leiomyomatosis and Renal Cell Cancer
- Hereditary Melanoma
- Hereditary Methemoglobinemia
- Hereditary Motor and Sensory Neuropathy
- Hereditary Multiple Osteochondromas
- Hereditary Neuropathy With Liability to Pressure Palsies
- Hereditary Pancreatitis
- Hereditary Paraganglioma-pheochromocytoma
- Hereditary Renal Cell Carcinoma
- Hereditary Sensory and Autonomic Neuropathy
- Hereditary Sensory Neuropathy Type 1
- Hereditary Spastic Paraplegia
- Hereditary Spherocytosis
- Hermansky-Pudlak Syndrome
- Herpes Simiae (B Virus)
- Herpes Simplex Encephalitis
- Herpes Zoster Ophthalmicus
- Herpes Zoster Oticus
- Heterotaxy
- Hidradenocarcinoma
- Hirschsprung Disease
- His Bundle Tachycardia
- HIVEP2-related Intellectual Disability
- Hodgkin Lymphoma
- Holoprosencephaly
- Homocysteinemia
- Homocystinuria
- Homocystinuria Due to CBS Deficiency
- Homologous Wasting Disease
- Horizontal Gaze Palsy With Progressive Scoliosis
- Horner's Syndrome
- Hoyeraal Hreidarsson Syndrome
- HTLV-1 Associated Myelopathy/tropical Spastic Paraparesis
- Human HOXA1 Syndromes
- Human T-cell Leukemia Virus Type 1
- Human T-cell Leukemia Virus Type 2
- Huntington Disease
- Hurler–Scheie Syndrome
- Hurler Syndrome
- Hurthle Cell Thyroid Cancer
- Hyaline Fibromatosis Syndrome
- Hydatidiform Mole
- Hydatidosis
- Hydrops Fetalis
- Hyperacusis
- Hyperadrenalism
- Hypereosinophilic Syndrome
- Hyper-IgD Syndrome
- Hyper IgE Syndrome
- Hyperinsulinism-hyperammonemia Syndrome
- Hyperkalemic Periodic Paralysis
- Hyperlipidemia Type 3
- Hyperlipoproteinemia Type 4
- Hyperlipoproteinemia Type 5
- Hypermobile Ehlers-Danlos Syndrome
- Hyperprolinemia
- Hypersensitivity Pneumonitis
- Hypersensitivity Vasculitis
- Hypoaldosteronism
- Hypochondroplasia
- Hypocomplementemic Urticarial Vasculitis
- Hypoganglionosis
- Hypohidrotic Ectodermal Dysplasia
- Hypokalemic Periodic Paralysis
- Hypolipoproteinemia
- Hypomelanotic Disorder
- Hypoparathyroidism
- Hypopharyngeal Cancer
- Hypophosphatasia
- Hypophosphatemic Rickets
- Hypopituitarism
- Hypoplastic Left Heart Syndrome
- Hypoplastic Right Heart Syndrome
- Hypothalamic Obesity
- Hypotrichosis Simplex
- Hypoxanthine Guanine Phosphoribosyltransferase Deficiency
- IBMPFD
- I Cell Disease
- Ichthyosis Linearis Circumflexa
- Ichthyosis Vulgaris
- Idiopathic Achalasia
- Idiopathic CD4 Positive T-lymphocytopenia
- Idiopathic Hypersomnia
- Idiopathic Inflammatory Myopathy
- Idiopathic Intracranial Hypertension
- Idiopathic Pulmonary Fibrosis
- Idiopathic Pulmonary Hemosiderosis
- Idiopathic Subglottic Tracheal Stenosis
- Idiopathic Thrombocytopenic Purpura
- IgA Nephropathy
- IgG4-related Disease
- Immune Thrombocytopenia
- Immunodeficiency With Hyper IgM Type 1
- Impairment of Oral Perception
- Imperforate Anus
- Inborn Amino Acid Metabolism Disorder
- Inclusion Body Myopathy 2
- Inclusion Body Myositis
- Inclusion Conjunctivitis
- Incontinentia Pigmenti
- Indolent B Cell Lymphoma
- Infantile Apnea
- Infantile Myofibromatosis
- Infantile Neuroaxonal Dystrophy
- Infantile Neuronal Ceroid Lipofuscinosis
- Infantile-onset Ascending Hereditary Spastic Paralysis
- Infantile Scoliosis