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Hailey-Hailey Disease
Haim-Munk Syndrome
Hairy Cell Leukemia
Hajdu Cheney Syndrome
Hallermann Streiff Syndrome
Hanhart Syndrome
Hantavirus Pulmonary Syndrome
Harlequin Ichthyosis
Hartnup Disease
Hashimoto Encephalopathy
Heavy Metal Poisoning
Hemimegalencephaly
Hemiplegic Migraine
Hemophagocytic Lymphohistiocytosis
Hemophilia A
Hemophilia B
Henoch-Schönlein Purpura
Hepatic Encephalopathy
Hepatocellular Carcinoma
Hepatoerythropoietic Porphyria
Hepatopulmonary Syndrome
Hepatorenal Syndrome
Hereditary Angioedema
Hereditary Breast and Ovarian Cancer Syndrome
Hereditary Coproporphyria
Hereditary Hemorrhagic Telangiectasia
Hereditary Hyperphosphatasia
Hereditary Leiomyomatosis and Renal Cell Carcinoma
Hereditary Lymphedema
Hereditary Multiple Osteochondromas
Hereditary Neuralgic Amyotrophy
Hereditary Nonspherocytic Hemolytic Anemia
Hereditary Orotic Aciduria
Hereditary Sensory and Autonomic Neuropathy Type 1E
Hereditary Sensory and Autonomic Neuropathy Type II
Hereditary Sensory and Autonomic Neuropathy Type IV
Hereditary Sensory Neuropathy Type I
Hereditary Spastic Paraplegia
Hereditary Spherocytosis
Hermansky Pudlak Syndrome
Herpes, Neonatal
Hiccups, Chronic
Hidradenitis Suppurativa
Hirschsprung Disease
Histidinemia
Hodgkin’s Disease
Holoprosencephaly
Holt Oram Syndrome
Homocystinuria due to Cystathionine Beta-Synthase Deficiency
Horner’s Syndrome
HTLV Type I and Type II
Human Granulocytic Ehrlichiosis (HGE)
Human HOXA1 Syndromes
Human Monocytic Ehrlichiosis (HME)
Huntington’s Disease
Hutchinson-Gilford Progeria Syndrome
Hydranencephaly
Hydrocephalus
Hyper IgM Syndromes
Hyperekplexia
Hyperemesis Gravidarum
Hyperferritinemia Cataract Syndrome
Hyperhidrosis, Primary
Hyperlipoproteinemia Type III
Hyperostosis Frontalis Interna
Hyperprolinemia Type I
Hyperprolinemia Type II
Hypochondroplasia
Hypohidrotic Ectodermal Dysplasia
Hypokalemia
Hypomelanosis of Ito
Hypoparathyroidism
Hypophosphatasia
Hypoplastic Left Heart Syndrome
Hypothalamic Hamartoma
