hypersensitivity pneumonitis; alveolitis

An interstitial lung disease involving inflammatio..[+]

An interstitial lung disease involving inflammation of alveoli and smallest airways (bronchioles) of the lung caused by an allergic reaction to inhaled organic dusts containing microorganisms or proteins, and chemicals. Symptoms include chills, cough, fever, malaise, shortness of breath, loss of appetite and weight loss. [-]

hepatolenticular degeneration; Westphal pseudoscle.. [+]

hepatolenticular degeneration; Westphal pseudosclerosis; Westphal-Strumpell syndrome; Cerebral pseudosclerosis; Wilson's disease [-]

A metal metabolism disease that is characterized b..[+]

A metal metabolism disease that is characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes. [-]

hyperkinetic disorder; ADHD; attention deficit dis.. [+]

hyperkinetic disorder; ADHD; attention deficit disorder [-]

A specific developmental disorder that is characte..[+]

A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age. [-]

Hench's syndrome; Hench-Rosenberg syndrome

An arthritis that involves sudden and rapidly deve..[+]

An arthritis that involves sudden and rapidly developing attacks of arthritis with a remission period that results_in no joint damage or symptoms. [-]

hypersensitivity reaction type I disease; hypersen.. [+]

hypersensitivity reaction type I disease; hypersensitivity; allergic disease; allergy; allergic hypersensitivity disease [-]

An immune system disease that is an exaggerated im..[+]

An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods. [-]

heat rash; eccrine miliaria; sweat rash

A sweat gland disease that is characterized by blo..[+]

A sweat gland disease that is characterized by blocked eccrine sweat glands and ducts. [-]

hydatid disease; hydatidosis; hepatic echinococcos.. [+]

hydatidosis; hydatid disease; hepatic echinococcosis; Echinococcosis, unspecified, of liver (disorder); Liver echinococcus unspecified (disorder); Echinococcosis of liver (disorder); Echinococcosis, unspecified, of liver; pulmonary echinococcosis; echinococcal disease; Echinococcosis of liver; liver echinococcus [-]

A parasitic helminthiasis infectious disease that ..[+]

A parasitic helminthiasis infectious disease that involves parasitic infection of humans and domestic animals caused by the larval stages of tapeworms of the genus Echinococcus in the liver, lungs, spleen, brain, heart and kidneys. [-]

Hysterical neurosis, conversion type; Conversion h.. [+]

Hysterical neurosis, conversion type; Conversion hysteria or reaction; Conversion Hysterical Neurosis [-]

A somatoform disorder that involves numbness, blin..[+]

A somatoform disorder that involves numbness, blindness, paralysis or fits without a neurological cause. [-]

hemangiosarcoma

A vascular cancer that derives_from the cells that..[+]

A vascular cancer that derives_from the cells that line the walls of blood vessels or lymphatic vessels. [-]

Hepatoid yolk sac tumour; Yolk sac tumor; infantil.. [+]

Hepatoid yolk sac tumour; Yolk sac tumor; infantile embryonal carcinoma; Yolk Sac neoplasm; Yolk sac tumour; endodermal sinus tumour; yolk sac tumor [-]

A germ cell cancer that has_material_basis_in cell..[+]

A germ cell cancer that has_material_basis_in cells that line the yolk sac of the embryo. [-]

Hypogonadotropic Hypogonadism; Klinefelter syndrom.. [+]

Hypogonadotropic Hypogonadism; Klinefelter syndrome; XXY syndrome; XXY trisomy; 47, XXY; Klinefelter's syndrome [-]

A chromosomal duplication syndrome that is charact..[+]

A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men. [-]

Hereditary factor XIII deficiency disease; Heredit.. [+]

Hereditary factor XIII deficiency disease; Hereditary factor XIII deficiency disease (disorder); Factor XIII deficiency disease (disorder); Factor XIII deficiency disease; deficiency, Laki-Lorand factor [-]

A blood coagulation disease that is characterized ..[+]

A blood coagulation disease that is characterized by easy bleeding, has_symptom prolonged umbilical cord bleeding, epistaxis, bleeding of the gums, menorrhagia, recurrent miscarriages, abnormal scar formation and wound healing, and hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation of the F13A1 or F13B gene, which encodes Factor XIII, formally known as fibrin stabilizing factor. [-]

Hemorrhagic dystrophic thrombocytopenia; Bernard -.. [+]

Hemorrhagic dystrophic thrombocytopenia; Bernard - Soulier thrombopathy; Bernard Soulier syndrome; Thrombopathy, Bernard-Soulier; Giant platelet syndrome (disorder); Giant platelet syndrome [-]

A blood coagulation disease characterized by autos..[+]

A blood coagulation disease characterized by autosomal recessive inheritance of mucosal bleeding, purpuric skin bleeding, epistaxis, and menorrhagia with prolonged bleeding times, enlarged platelets and absence of platelet aggregation in response to von Willebrand factor that has_material_basis_in mutation in the GP1BA gene, the GP1BB gene, or the GP9 gene which are subunits of the platelet membrane von Willebrand factor receptor complex, glycoprotein Ib. [-]

hemophilia C; Hereditary factor XI deficiency dise.. [+]

hemophilia C; Hereditary factor XI deficiency disease; plasma thromboplastin antecedent deficiency; Rosenthal's disease; Congenital factor XI deficiency [-]

A blood coagulation disease that is characterized ..[+]

A blood coagulation disease that is characterized by deficiency of factor XI clotting factor and mild prolonged bleeding, especially of mucosal sites following trauma, and has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation of the coagulation factor XI gene of chromosome 4q35.2. [-]

Hereditary factor II deficiency disease; hypoproth.. [+]

Hereditary factor II deficiency disease; hypoprothrombinemia; Factor II deficiency; Congenital factor II deficiency [-]

A thrombophilia that is characterized by bleeding ..[+]

A thrombophilia that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11. [-]

HSMN - Hereditary sensory and motor neuropathy; HS.. [+]

HSMN - Hereditary sensory and motor neuropathy; HSMN; Hereditary motor and sensory neuropathy; neuropathic muscular atrophy; Peripheral Motor Neuropathy [-]

A neuropathy that is characterized by inflammation..[+]

A neuropathy that is characterized by inflammation or degeneration of the peripheral motor nerves. [-]

Histiocytosis X; Langerhans cell granulomatosis; L.. [+]

Histiocytosis X; Langerhans cell granulomatosis; Letterer-Siwe disease; Letterer-Siwe disease involving intra-abdominal lymph nodes; Letterer-Siwe disease involving intrapelvic lymph nodes; Letterer-Siwe disease involving lymph nodes of axilla and upper limb; Letterer-Siwe disease involving lymph nodes of head, face and neck; Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb; Letterer-Siwe disease involving lymph nodes of multiple sites; Letterer-Siwe disease involving spleen; Letterer-Siwe disease of intra-abdominal lymph nodes; Letterer-Siwe disease of intrapelvic lymph nodes; Letterer-Siwe disease of intrapelvic lymph nodes (disorder); Letterer-Siwe disease of intrathoracic lymph nodes; Letterer-Siwe disease of lymph nodes of axilla and upper limb (disorder); Letterer-Siwe disease of lymph nodes of axilla and/or upper limb; Letterer-Siwe disease of lymph nodes of head, face and neck (disorder); Letterer-Siwe disease of lymph nodes of head, face and/or neck (disorder); Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb; Letterer-Siwe disease of lymph nodes of inguinal region and lower limb (disorder); Letterer-Siwe disease of lymph nodes of multiple sites; Letterer-Siwe disease of lymph nodes of multiple sites (disorder); Letterer-Siwe disease of spleen; Letterer-Siwe disease of spleen (disorder); Langerhan's cell histiocytosis (disorder); Letterer-Siwe disease involving intrathoracic lymph nodes; Letterer-Siwe disease involving lymph nodes of head, face, and neck; Letterer-Siwe disease of intra-abdominal lymph nodes (disorder); Letterer-Siwe disease of intrathoracic lymph nodes (disorder); Letterer-Siwe disease of lymph nodes of axilla and/or upper limb (disorder); Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb (disorder); Langerhan's cell histiocytosis; Letterer-Siwe disease of lymph nodes of axilla and upper limb; Letterer-Siwe disease of lymph nodes of head, face and neck; Letterer-Siwe disease of lymph nodes of head, face and/or neck; Letterer-Siwe disease of lymph nodes of inguinal region and lower limb; Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb [-]

A histiocytosis that is characterized by clonal pr..[+]

A histiocytosis that is characterized by clonal proliferation of Langerhans cells. [-]

hereditary nonhemolytic jaundice; Constitutional h.. [+]

hereditary nonhemolytic jaundice; Constitutional hyperbilirubinemia; Gilbert's disease; Gilbert-Meulengracht syndrome; Gilbert's syndrome [-]

A bilirubin metabolic disorder that involves eleva..[+]

A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity. [-]

hepatic glycogen phosphorylase kinase deficiency; .. [+]

hepatic glycogen phosphorylase kinase deficiency; hepatic glycogen phosphorylase kinase deficiency (disorder); Glycogen storage disease type VIII (disorder); glycogenosis type VIII; glycogen storage disease type VIII; Glycogen storage disease type VIII; Glycogen storage disease 8 [-]

A glycogen storage disease that is characterized h..[+]

A glycogen storage disease that is characterized hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase and results from the lack of expression of phosphorylase-b-kinase activity. [-]

Hamman-Rich syndrome; Hamman-Rich disease; acceler.. [+]

Hamman-Rich disease; Hamman-Rich syndrome; accelerated interstitial pneumonia; acute interstitial pneumonitis; AIP; Idiopathic pulmonary fibrosis, acute fatal form [-]

A idiopathic interstitial pneumonia which develops..[+]

A idiopathic interstitial pneumonia which develops suddenly and is severe. Initially, the lung shows edema, hyaline membranes, and interstitial acute inflammation. Later, it develops loose organizing fibrosis, mostly within alveolar septa and type II pneumocyte hyperplasia. Fever, cough, and difficulty breathing develop over 1 to 2 weeks, typically progressing to acute respiratory failure. [-]

HEMIFACIAL MICROSOMIA; Facio-auriculo-vertebral sp.. [+]

HEMIFACIAL MICROSOMIA; Facio-auriculo-vertebral spectrum (disorder); First AND second branchial arch syndrome; First arch syndrome (disorder); Otomandibular dysostosis (disorder); OAV (oculoauriculovertebral) dysplasia; Facio-auriculo-vertebral spectrum; First arch syndrome; Otomandibular dysostosis [-]

A syndrome that is characterized by incomplete dev..[+]

A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch. [-]

hepatic porphyria; hepatic porphyria (disorder)

A porphyria that has_symptom abdominal pain, has_s..[+]

A porphyria that has_symptom abdominal pain, has_symptom neuropathy, has_symptom autonomic instability and has_symptom psychosis. [-]

HLD1; hypomyelinating leukodystrophy 1; Leukodystr.. [+]

hypomyelinating leukodystrophy 1; HLD1; Leukodystrophy, sudanophilic; Pelizaeus Merzbacher brain sclerosis; Pelizaeus-Merzbacher brain sclerosis; sudanophilic leukodystrophy, Paelizeus-Merzbacher type; diffuse familial brain sclerosis; PMD [-]

A hypomyelinating leukodystrophy characterized by ..[+]

A hypomyelinating leukodystrophy characterized by impaired myelin formation, nystagmus, spastic quadriplegia, ataxia, and developmental delay that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22. [-]

hyperparathyroid bone disease; Osteitis fibrosa cy.. [+]

hyperparathyroid bone disease; Osteitis fibrosa cystica generalisata (disorder); Von Recklinghausen's bone disease; Osteitis fibrosa cystica generalisata [-]

A bone resorption disease that has_material_basis_..[+]

A bone resorption disease that has_material_basis_in hyperparathyroidism which results_in hyperactivity in osteoclasts, deformity, and loss of mass located_in bone. [-]

hepatic cancer; hepatic neoplasm; ca liver - prima.. [+]

hepatic neoplasm; hepatic cancer; ca liver - primary; Ca liver - primary (disorder); malignant hepato-biliary neoplasm; malignant neoplasm of liver (disorder); malignant neoplasm of liver unspecified (disorder); malignant neoplasm of liver, primary; malignant tumor of liver (disorder); non-resectable primary hepatic malignant neoplasm; primary liver cancer; primary malignant neoplasm of liver; primary malignant neoplasm of liver NOS (disorder); malignant neoplasm of liver; neoplasm of liver (disorder); primary malignant neoplasm of liver (disorder); Ca liver - primary; malignant tumor of liver; resectable malignant neoplasm of the liver; malignant neoplasm of liver, not specified as primary or secondary; Resectable malignant neoplasm of Liver; primary malignant neoplasm of Liver; neoplasm of liver [-]

A hepatobiliary system cancer that is located_in t..[+]

A hepatobiliary system cancer that is located_in the liver. [-]