List of diseases (H)
This is a list of diseases starting with the letter "H".
Ha
Hag–Ham
- Hageman factor deficiency[1]
- Hagemoser–Weinstein–Bresnick syndrome
- Hailey–Hailey disease
- Hair defect with photosensitivity and mental retardation
- Hairy cell leukemia[2]
- Hairy ears, y-linked
- Hairy ears
- Hairy nose tip
- Hairy palms and soles
- Hairy tongue
- Hajdu–Cheney syndrome[3]
- Halal–Setton–Wang syndrome
- Halal syndrome
- Hall–Riggs mental retardation syndrome
- Hallermann–Streiff syndrome[4]
- Hallervorden–Spatz disease (renamed to Pantothenate kinase-associated neurodegeneration due to Hallervorden's Nazi party associations)
- Hallucinogen persisting perception disorder
- Hallux valgus
- Hamanishi–Ueba–Tsuji syndrome
- Hamano–Tsukamoto syndrome
- Hamartoma sebaceus of Jadassohn
Han–Hay
- Hantavirus
- Hantavirus pulmonary syndrome[5]
- Hand and foot deformity flat facies
- Hand–foot–uterus syndrome
- Hand wringing Rett syndrome
- Hand, foot and mouth disease
- Hand–Schüller–Christian disease
- Hanhart syndrome[6]
- Harding ataxia
- Harlequin type ichthyosis (Also Known As Harlequin Ichthyosis)
- Harpaxophobia
- Harrod–Doman–Keele syndrome
- Hartnup disease[7]
- Hartsfield–Bixler–Demyer syndrome
- Hashimoto struma
- Hashimoto–Pritzker syndrome
- Hashimoto's thyroiditis
- Haspeslagh–Fryns–Muelenaere syndrome
- Hay–Wells syndrome recessive type
- Hay–Wells syndrome
He
Hea–Hei
- Headache, cluster
- Hearing disorder
- Hearing impairment
- Hearing loss
- Heart aneurysm
- Heart attack[8]
- Heart block progressive, familial
- Heart block[9]
- Heart defect round face congenital retarded development
- Heart defect tongue hamartoma polysyndactyly
- Heart defects limb shortening
- Heart hand syndrome Spanish type
- Heart hypertrophy, hereditary
- Heart situs anomaly
- Heart tumor of the adult
- Heart tumor of the child
- Heavy metal poisoning
- HEC syndrome
- Hecht–Scott syndrome
- Heckenlively syndrome
- Heide syndrome
Hel
- Heliophobia
- HELLP syndrome
- Helmerhorst–Heaton–Crossen syndrome
- Helminthiasis
Hem
- HEM dysplasia
Hema–Hemi
- Hemangioblastoma[10]
- Hemangioendothelioma[11]
- Hemangioma thrombocytopenia syndrome
- Hemangioma, capillary infantile
- Hemangioma
- Hemangiomatosis, familial pulmonary capillary
- Hemangiopericytoma
- Hematocolpos[12]
- Hemeralopia, congenital essential
- Hemeralopia, familial
- Hemi 3 syndrome[13]
- Hemifacial atrophy agenesis of the caudate nucleus
- Hemifacial atrophy progressive
- Hemifacial hyperplasia strabismus
- Hemifacial microsomia
- Hemihypertrophy in context of NF
- Hemihypertrophy intestinal web corneal opacity
- Hemimegalencephaly[14]
- Hemiplegia
- Hemiplegic migraine, familial
Hemo
- Hemochromatosis
- Hemoglobin C disease[15]
- Hemoglobin E disease[16]
- Hemoglobin SC disease[17]
- Hemoglobinopathy
- Hemoglobinuria
- Hemolytic anemia lethal genital anomalies
- Hemolytic-uremic syndrome[18]
- Hemophagocytic lymphohistiocytosis[19]
- Hemophagocytic reticulosis[20]
- Hemophilia A[21]
- Hemophilia B[22]
- Hemophilic arthropathy
- Hemophobia
- Hemorrhagic fever with renal syndrome
- Hemorrhoid
- Hemorrhagic proctocolitis
- Hemorrhagic thrombocythemia
- Hemorrhagiparous thrombocytic dystrophy
- Hemosiderosis[23]
- Hemothorax
Hen
- Hennekam–Beemer syndrome
- Hennekam–Koss–de Geest syndrome
- Hennekam syndrome
- Hennekam–Van der Horst syndrome
- Henoch–Schönlein purpura
Hep
- Hepadnovirus D
- Heparane sulfamidase deficiency
- Heparin-induced thrombopenia
- Hepatic cystic hamartoma
- Hepatic ductular hypoplasia
- Hepatic encephalopathy
- Hepatic fibrosis renal cysts mental retardation
- Hepatic fibrosis
- Hepatic venoocclusive disease
- Hepatic veno-occlusive disease
- Hepatitis
- Hepatitis A
- Hepatitis B
- Hepatitis C
- Hepatitis D
- Hepatitis E
- Hepatoblastoma[24]
- Hepatocellular carcinoma[25]
- Hepatorenal syndrome
- Hepatorenal tyrosinemia
Her
Here
Hered
Heredi
Hereditary a – Hereditary m
- Hereditary amyloidosis
- Hereditary angioedema
- Hereditary ataxia
- Hereditary breast–ovarian cancer syndrome
- Hereditary carnitine deficiency myopathy
- Hereditary carnitine deficiency syndrome
- Hereditary carnitine deficiency
- Hereditary ceroid lipofuscinosis
- Hereditary coproporphyria
- Hereditary deafness
- Hereditary elliptocytosis[26]
- Hereditary fibrinogen Aα-Chain amyloidosis
- Hereditary fructose intolerance
- Hereditary hearing disorder
- Hereditary hearing loss
- Hereditary hemochromatosis
- Hereditary hemorrhagic telangiectasia
- Hereditary hyperuricemia
- Hereditary macrothrombocytopenia[27]
- Hereditary methemoglobinemia, recessive
- Hereditary myopathy with intranuclear filamentous
Hereditary n – Hereditary t
- Hereditary nodular heterotopia
- Hereditary non-spherocytic hemolytic anemia
- Hereditary pancreatitis
- Hereditary paroxysmal cerebral ataxia
- Hereditary peripheral nervous disorder
- Hereditary primary Fanconi disease
- Hereditary resistance to anti-vitamin K
- Hereditary sensory and autonomic neuropathy 3
- Hereditary sensory and autonomic neuropathy 4
- Hereditary sensory neuropathy type I
- Hereditary sensory neuropathy type II
- Hereditary spastic paraplegia
- Hereditary spherocytic hemolytic anemia
- Hereditary spherocytosis[28]
- Hereditary type 1 neuropathy
- Hereditary type 2 neuropathy
Herm–Hers
- Hermansky–Pudlak syndrome
- Hermaphroditism
- Hernandez–Aguire–Negrete syndrome
- Herpangina
- Herpes encephalitis
- Herpes simplex disease
- Herpes simplex encephalitis
- Herpes viridae disease
- Herpes virus antenatal infection
- Herpes zoster oticus
- Herpes zoster
- Herpesvirus simiae B virus
- Herpetic embryopathy
- Herpetic keratitis
- Herpetophobia
- Herrmann–Opitz arthrogryposis syndrome
- Herrmann–Opitz craniosynostosis
- Hers' disease
- Hersh–Podruch–Weisskopk syndrome
Het–Hex
Hh
Hi
Hib–Hip
- Hibernian fever, familial
- Hiccups
- Hidradenitis suppurativa familial
- Hidradenitis suppurativa
- Hidrotic ectodermal dysplasia type Christianson Fouris
- High scapula
- High-molecular-weight kininogen deficiency, congenital
- Hillig syndrome
- Hing–Torack–Dowston syndrome
- Hinson–Pepys disease
- Hip dislocation
- Hip dysplasia Beukes type
- Hip dysplasia (canine)
- Hip dysplasia (human)
- Hip luxation
- Hip subluxation
- Hipo syndrome
Hir–Hiv
- Hirschsprung disease[29]
- Hirschsprung disease ganglioneuroblastoma
- Hirschsprung disease polydactyly heart disease
- Hirschsprung disease type 2
- Hirschsprung disease type 3
- Hirschsprung disease type d brachydactyly
- Hirschsprung microcephaly cleft palate
- Hirschsprung nail hypoplasia dysmorphism
- Hirsutism congenital gingival hyperplasia
- Hirsutism skeletal dysplasia mental retardation
- His bundle tachycardia
- Histadelia
- Histapenia
- Histidinemia
- Histidinuria renal tubular defect syndrome
- Histiocytosis X[30]
- Histiocytosis, Non-Langerhans-Cell
- Histoplasmosis[31]
- Histrionic personality disorder
- Hittner–Hirsch–Kreh syndrome
- HIV
Hm
Ho
Hod–Hol
- Hodgkin lymphoma[33]
- Hodgkin's disease
- Hoepffner–Dreyer–Reimers syndrome
- Hollow visceral myopathy
- Holmes–Benacerraf syndrome
- Holmes–Borden syndrome
- Holmes–Collins syndrome
- Holmes–Gang syndrome
- Holoacardius amorphus
- Holocarboxylase synthetase deficiency
- Holoprosencephaly caudal dysgenesis
- Holoprosencephaly deletion 2p
- Holoprosencephaly ectrodactyly cleft lip palate
- Holoprosencephaly radial heart renal anomalies
- Holoprosencephaly
- Holt–Oram syndrome[34]
- Holzgreve–Wagner–Rehder syndrome
Hom–Hoy
- Homocarnosinase deficiency
- Homocarnosinosis
- Homocystinuria due to cystathionine beta-synthase
- Homocystinuria due to defect in methylation (cbl g)
- Homocystinuria due to defect in methylation cbl e
- Homocystinuria due to defect in methylation, MTHFR deficiency
- Homocystinuria[35]
- Homologous wasting disease
- Homozygous hypobetalipoproteinemia
- Hoon–Hall syndrome
- Hordnes–Engebretsen–Knudtson syndrome
- Horn–Kolb syndrome
- Horner's syndrome
- Hornova–Dlurosova syndrome
- Horseshoe kidney[36]
- Horton disease, juvenile
- Horton disease[37]
- Hot tub folliculitis[38]
- Houlston–Ironton–Temple syndrome
- Howard–Young syndrome
- Howel–Evans syndrome
- Hoyeraal–Hreidarsson syndrome
- Hoyeraal syndrome
Hs
Hu
- Human ewingii ehrlichiosis
- Human granulocytic ehrlichiosis
- Human monocytic ehrlichiosis
- Human parvovirus B19 infection
- Humero spinal dysostosis congenital heart disease
- Humeroradial synostosis
- Humeroradioulnar synostosis
- Humerus trochlea aplasia of
- Hunter–Carpenter–Mcdonald syndrome
- Hunter–Jurenka–Thompson syndrome
- Hunter–Macpherson syndrome
- Hunter–Mcalpine syndrome
- Hunter–Mcdonald syndrome
- Hunter–Rudd–Hoffmann syndrome
- Hunter syndrome
- Huntington's disease
- Huriez scleroatrophic syndrome
- Hurler syndrome
- Hurst–Hallam–Hockey syndrome
- Hutchinson–Gilford–Progeria syndrome
- Hutchinson incisors
- Hutteroth–Spranger syndrome
Hy
Hya
Hyd
Hyda–Hyde
- Hydantoin antenatal infection
- Hydatidiform mole
- Hydatidosis
- Hyde–Forster–Mccarthy–Berry syndrome
Hydr
- Hydranencephaly
- Hydrocephalus - Arnold Chiari - allied disorders
- Hydrocephalus autosomal recessive
- Hydrocephalus costovertebral dysplasia Sprengel anomaly
- Hydrocephalus craniosynostosis bifid nose
- Hydrocephalus endocardial fibroelastosis cataract
- Hydrocephalus growth retardation skeletal anomalies
- Hydrocephalus obesity hypogonadism
- Hydrocephalus skeletal anomalies
- Hydrocephalus[39]
- Hydrocephaly corpus callosum agenesis diaphragmatic hernia
- Hydrocephaly low insertion umbilicus
- Hydrocephaly tall stature joint laxity
- Hydrolethalus syndrome
- Hydronephrosis
- Hydronephrosis peculiar facial expression
- Hydrophobia
- Hydrops ectrodactyly syndactyly
- Hydrops fetalis anemia immune disorder absent thumb
- Hydrops fetalis[40]
- Hydroxycarboxylic aciduria
- Hydroxymethylglutaric aciduria
Hyg-Hym
Hyp
Hyper
Hypera–Hyperb
Hyperc–Hyperg
- Hypercalcemia, familial benign type 1
- Hypercalcemia, familial benign type 2
- Hypercalcemia, familial benign type 3
- Hypercalcemia, familial benign
- Hypercalcemia
- Hypercalcinuria idiopathic
- Hypercalcinuria macular coloboma
- Hypercalcinuria
- Hypercementosis
- Hypercholesterolemia due to arg3500 mutation of Apo B-100
- Hypercholesterolemia due to LDL receptor deficiency
- Hypercholesterolemia
- Hyperchylomicronemia
- Hyperekplexia
- Hypereosinophilic syndrome
- Hyperferritinemia, hereditary, with congenital cataracts
- Hypergeusia
- Hyperglycemia
- Hyperglycerolemia
- Hyperglycinemia, isolated nonketotic type 1
- Hyperglycinemia, isolated nonketotic type 2
- Hyperglycinemia, isolated nonketotic
- Hyperglycinemia, ketotic
- Hyperglycinemia, non-ketotic
- Hypergonadotropic ovarian failure, familial or sporadic
Hyperh–Hyperk
- Hyperhidrosis
- Hyperhomocysteinemia
- Hyper-IgD syndrome
- Hyperimidodipeptiduria
- Hyperimmunoglobinemia D with recurrent fever
- Hyperimmunoglobulin E - recurrent infection syndrome
- Hyperimmunoglobulinemia D with periodic fever
- Hyperimmunoglobulinemia E
- Hyperinsulinism due to focal adenomatous hyperplasia
- Hyperinsulinism due to glucokinase deficiency
- Hyperinsulinism due to glutamodehydrogenase deficiency
- Hyperinsulinism in children, congenital
- Hyperinsulinism, diffuse
- Hyperinsulinism, focal
- Hyperkalemia
- Hyperkalemic periodic paralysis
- Hyperkeratosis lenticularis perstans of Flegel
- Hyperkeratosis lenticularis perstans
- Hyperkeratosis palmoplantar localized acanthokeratolytic
- Hyperkeratosis palmoplantar localized epidermolytic
- Hyperkeratosis palmoplantar with palmar crease hyperkeratosis
Hyperl–Hypero
- Hyperlipoproteinemia type I
- Hyperlipoproteinemia type II
- Hyperlipoproteinemia type III
- Hyperlipoproteinemia type IV
- Hyperlipoproteinemia type V
- Hyperlipoproteinemia
- Hyperlysinemia
- Hyperopia
- Hyperornithinemia
- Hyperornithinemia, hyperammonemia, homocitrullinuria syndrome
- Hyperostosid corticalis deformans juvenilis
- Hyperostosis cortical infantile
- Hyperostosis corticalis generalisata
- Hyperostosis frontalis interna
- Hyperoxaluria type 1
- Hyperoxaluria type 2
- Hyperoxaluria
Hyperp–Hypers
- Hyperparathyroidism
- Hyperparathyroidism, familial, primary
- Hyperparathyroidism, neonatal severe primary
- Hyperphalangism dysmorphy bronchomalacia
- Hyperphenylalaninemia
- Hyperphenylalaninemia due to pterin-4-alpha-carbin
- Hyperphenylalaninemia due to dihydropteridine reductase deficiency
- Hyperphenylalaninemia due to 6-pyruvoyltetrahydrop
- Hyperphenylalaninemia due to dehydratase deficiency
- Hyperphenylalaninemia due to GTP cyclohydrolase deficiency
- Hyperphenylalaninemic embryopathy
- Hyperpipecolatemia
- Hyperprolactinemia
- Hyperprolinemia type II
- Hyperprolinemia
- Hyperreflexia
- Hyper-reninism
- Hypersensitivity
Hypert–Hyperv
- Hypertelorism and tetralogy of Fallot
- Hypertelorism hypospadias syndrome
- Hypertension
- Hypertensive hyperkalemia, familial
- Hypertensive hypokalemia familial
- Hypertensive retinopathy
- Hyperthermia induced defects
- Hyperthermia
- Hyperthyroidism
- Hyperthyroidism due to mutations in TSH receptor
- Hypertrichosis atrophic skin ectropion macrostomia
- Hypertrichosis brachydactyly obesity and mental retardation
- Hypertrichosis congenital generalized X linked
- Hypertrichosis lanuginosa congenita
- Hypertrichosis lanuginosa, acquired
- Hypertrichosis retinopathy dysmorphism
- Hypertrichosis, anterior cervical
- Hypertrichotic osteochondrodysplasia
- Hypertriglycidemia
- Hypertrophic branchial myopathy
- Hypertrophic cardiomyopathy
- Hypertrophic hemangiectasia
- Hypertrophic myocardiopathy
- Hypertrophic osteoarthropathy, primary or idiopathic
- Hypertropia
- Hypertropic neuropathy of Dejerine-Sottas
- Hypertryptophanemia
- Hypervitaminosis A
- Hypervitaminosis D
- Hypervitaminosis E
Hypo
Hypoa–Hypof
- Hypoactive sexual desire disorder
- Hypoadrenalism
- Hypoadrenocorticism hypoparathyroidism moniliasis
- Hypoaldosteronism
- Hypo-alphalipoproteinemia primary
- Hypobetalipoproteinaemia ataxia hearing loss
- Hypobetalipoprotéinemia, familial
- Hypocalcemia, autosomal dominant
- Hypocalcemia
- Hypocalciuric hypercalcemia, familial
- Hypochondriasis
- Hypochondrogenesis
- Hypochondroplasia
- Hypocomplementemic urticarial vasculitis
- Hypodermyasis
- Hypodontia dysplasia of nails
- Hypodontia of incisors and premolars
- Hypodysfibrinogenemia
- Hypofibrinogenemia, familial
Hypog–Hypol
- Hypoglycemia with deficiency of glycogen synthetase in the liver
- Hypoglycemia
- Hypogonadism cardiomyopathy
- Hypogonadism hypogonadotropic due to mutations in GR hormone
- Hypogonadism male mental retardation skeletal anomaly
- Hypogonadism mitral valve prolapse mental retardation
- Hypogonadism primary partial alopecia
- Hypogonadism retinitis pigmentosa
- Hypogonadism, isolated, hypogonadotropic
- Hypogonadism
- Hypogonadotropic hypogonadism syndactyly
- Hypogonadotropic hypogonadism without anosmia, X linked
- Hypogonadotropic hypogonadism-anosmia, X linked
- Hypogonadotropic hypogonadism-anosmia
- Hypohidrotic Ectodermal Dysplasia
- Hypokalemia
- Hypokalemic alkalosis with hypercalcinuria
- Hypokalemic periodic paralysis
- Hypokalemic periodic paralysis type 1
- Hypokalemic sensory overstimulation
- Hypoketonemic hypoglycemia
- Hypolipoproteinemia
Hypom
- Hypomagnesemia primary
- Hypomandibular faciocranial dysostosis
- Hypomelanotic disorder
- Hypomelia Müllerian duct anomalies
- Hypomentia
Hypop
- Hypoparathyroidism familial isolated
- Hypoparathyroidism nerve deafness nephrosis
- Hypoparathyroidism short stature mental retardation
- Hypoparathyroidism short stature
- Hypoparathyroidism X linked
- Hypoparathyroidism
- Hypophosphatasia, infantile
- Hypophosphatasia
- Hypophosphatemic rickets
- Hypopigmentation oculocerebral syndrome Cross type
- Hypopituitarism micropenis cleft lip palate
- Hypopituitarism postaxial polydactyly
- Hypopituitarism
- Hypopituitary dwarfism
- Hypoplasia hepatic ductular
- Hypoplasia of the tibia with polydactyly
- Hypoplastic left heart syndrome
- Hypoplastic right heart microcephaly
- Hypoplastic thumb Müllerian aplasia
- Hypoplastic thumbs hydranencephaly
- Hypoproconvertinemia
- Hypoprothrombinemia
Hypor–Hypox
- Hyporeninemic hypoaldosteronism
- Hyposmia nasal hypoplasia hypogonadism
- Hypospadias familial
- Hypospadias mental retardation Goldblatt type
- Hyposplenism
- Hypotelorism cleft palate hypospadias
- Hypothalamic dysfunction
- Hypothalamic hamartoblastoma syndrome
- Hypothalamic hamartomas
- Hypertonic gingivitus
- Hypothermia
- Hypothyroidism due to iodide transport defect
- Hypothyroidism postaxial polydactyly mental retardation
- Hypothyroidism
- Hypotonic sclerotic muscular dystrophy
- Hypotrichosis mental retardation Lopes type
- Hypotrichosis
- Hypotropia
- Hypoxanthine guanine phosphoribosyltransferase deficiency
- Hypoxia
References
- ↑ Chaudhry, Liaqat Ali; El-Sadek, Wael Yasin Mohamed; Chaudhry, Ghazala Aslam; Al-Atawi, Feddha Eid (2019). "Factor XII (Hageman Factor) Deficiency: a rare harbinger of life threatening complications". The Pan African Medical Journal. 33: 39. doi:10.11604/pamj.2019.33.39.18117. ISSN 1937-8688. PMC 6658145. PMID 31384354.
- ↑ Troussard, Xavier; Maître, Elsa; Paillassa, Jérôme (2024). "Hairy cell leukemia 2024: Update on diagnosis, risk-stratification, and treatment-Annual updates in hematological malignancies". American Journal of Hematology. 99 (4): 679–696. doi:10.1002/ajh.27240. ISSN 1096-8652. PMID 38440808.
- ↑ Cortés-Martín, Jonathan; Díaz-Rodríguez, Lourdes; Piqueras-Sola, Beatriz; Rodríguez-Blanque, Raquel; Bermejo-Fernández, Antonio; Sánchez-García, Juan Carlos (2020-08-25). "Hajdu-Cheney Syndrome: A Systematic Review of the Literature". International Journal of Environmental Research and Public Health. 17 (17): 6174. Bibcode:2020IJERP..17.6174C. doi:10.3390/ijerph17176174. ISSN 1660-4601. PMC 7504254. PMID 32854429.
- ↑ Thomas, Jayakar; Ragavi, B. Sindhu; Raneesha, Pk; Ahmed, N. Ashwak; Cynthia, S.; Manoharan, D.; Manoharan, R. (2013). "Hallermann-streiff syndrome". Indian Journal of Dermatology. 58 (5): 383–384. doi:10.4103/0019-5154.117311. ISSN 1998-3611. PMC 3778780. PMID 24082185.
- ↑ Moore, Ross A.; Griffen, David (2026), "Hantavirus Pulmonary Syndrome", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30020615, retrieved 2026-08-21
- ↑ Varal, Ipek Guney; Dogan, Pelin (2019). "Hanhart syndrome: hypoglossia-hypodactylia syndrome". The Pan African Medical Journal. 32: 213. doi:10.11604/pamj.2019.32.213.17493. ISSN 1937-8688. PMC 6620079. PMID 31312325.
- ↑ Hashmi, Mydah S.; Gupta, Vikas (2026), "Hartnup Disease", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32644502, retrieved 2026-08-24
- ↑ Ojha, Niranjan; Dhamoon, Amit S. (2026), "Myocardial Infarction", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30725761, retrieved 2026-08-21
- ↑ Oldroyd, Sean H.; Quintanilla Rodriguez, Bryan S.; Makaryus, Amgad N. (2026), "First-Degree Heart Block", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 28846254, retrieved 2026-08-21
- ↑ Khan, Muhammad M.; Hall, Walter A.; Belkhair, Sirajeddin (2026), "Hemangioblastoma", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 39163468, retrieved 2026-08-23
- ↑ Stacchiotti, S.; Miah, A. B.; Frezza, A. M.; Messiou, C.; Morosi, C.; Caraceni, A.; Antonescu, C. R.; Bajpai, J.; Baldini, E.; Bauer, S.; Biagini, R.; Bielack, S.; Blay, J. Y.; Bonvalot, S.; Boukovinas, I. (2021). "Epithelioid hemangioendothelioma, an ultra-rare cancer: a consensus paper from the community of experts". ESMO Open. 6 (3) 100170. doi:10.1016/j.esmoop.2021.100170. ISSN 2059-7029. PMC 8182432. PMID 34090171.
- ↑ Jason, M.; Capelle, X.; Raquet, J.; Kridelka, F. (2017). "[Hematocolpos : an unappreciated diagnosis of hymen imperforation]". Revue Medicale De Liege. 72 (11): 478–481. ISSN 0370-629X. PMID 29171945.
- ↑ Nudleman, K.; Andermann, E.; Andermann, F.; Bertrand, G.; Rogala, E. (1984). "The hemi 3 syndrome. Hemihypertrophy, hemihypaesthesia, hemiareflexia and scoliosis". Brain: A Journal of Neurology. 107 ( Pt 2): 533–546. doi:10.1093/brain/107.2.533. ISSN 0006-8950. PMID 6722516.
- ↑ Flores-Sarnat, L. (2007), Hemimegalencephaly syndrome, Handbook of Clinical Neurology, vol. 87, Elsevier, pp. 153–176, doi:10.1016/s0072-9752(07)87010-2, ISBN 978-0-444-51896-5, PMID 18809024, retrieved 2026-08-21
- ↑ Regragui, Ismail; Mamad, Hassane; El Mokhtari, Najoua; Woumki, Aziz; Dahmani, Fatima; Benkirane, Souad; Masrar, Azlarab (2025). "Hematological Profile of Hemoglobin C Disease: A Retrospective Study". Cureus. 17 (3) e80255. doi:10.7759/cureus.80255. ISSN 2168-8184. PMC 11975125. PMID 40196068.
- ↑ Fucharoen, Suthat; Weatherall, David J. (2012-08-01). "The hemoglobin E thalassemias". Cold Spring Harbor Perspectives in Medicine. 2 (8) a011734. doi:10.1101/cshperspect.a011734. ISSN 2157-1422. PMC 3405827. PMID 22908199.
- ↑ Nelson, M.; Noisette, L.; Pugh, N.; Gordeuk, V.; Hsu, L. L.; Wun, T.; Shah, N.; Glassberg, J.; Kutlar, A.; Hankins, J. S.; King, A. A.; Brambilla, D.; Kanter, J. (2024). "The clinical spectrum of HbSC sickle cell disease-not a benign condition". British Journal of Haematology. 205 (2): 653–663. doi:10.1111/bjh.19523. ISSN 1365-2141. PMC 11315634. PMID 38898714.
- ↑ Michael, Mini; Bagga, Arvind; Sartain, Sarah E.; Smith, Richard J. H. (2022-11-12). "Haemolytic uraemic syndrome". Lancet. 400 (10364): 1722–1740. doi:10.1016/S0140-6736(22)01202-8. ISSN 1474-547X. PMID 36272423.
- ↑ Konkol, Sam; Killeen, Robert B.; Rai, Maitreyee (2026), "Hemophagocytic Lymphohistiocytosis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32491708, retrieved 2026-08-24
- ↑ Standage, Stephen W.; Filipovich, Alexandra H. (2014), Wheeler, Derek S.; Wong, Hector R.; Shanley, Thomas P. (eds.), "Hemophagocytic Lymphohistiocytosis Syndromes", Pediatric Critical Care Medicine, London: Springer London, pp. 385–393, doi:10.1007/978-1-4471-6416-6_26, ISBN 978-1-4471-6415-9, PMC 7121621, retrieved 2026-08-24
{{citation}}: CS1 maint: work parameter with ISBN (link) - ↑ Sarmiento Doncel, Samuel; Díaz Mosquera, Gina Alejandra; Cortes, Javier Mauricio; Agudelo Rico, Carol; Meza Cadavid, Francisco Javier; Peláez, Ronald Guillermo (2023-02-16). "Haemophilia A: A Review of Clinical Manifestations, Treatment, Mutations, and the Development of Inhibitors". Hematology Reports. 15 (1): 130–150. doi:10.3390/hematolrep15010014. ISSN 2038-8322. PMC 9944491. PMID 36810557.
- ↑ Killeen, Robert B.; Rokkam, Venkata R. (2026), "Hemophilia B", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32809627, retrieved 2026-08-24
- ↑ Kayali, Zeid; Ranguelov, Rostislav; Mitros, Frank; Shufelt, Chrisandra; Elmi, Farshad; Rayhill, Stephen C.; Schmidt, Warren N.; Brown, Kyle E. (2005). "Hemosiderosis is associated with accelerated decompensation and decreased survival in patients with cirrhosis". Liver International: Official Journal of the International Association for the Study of the Liver. 25 (1): 41–48. doi:10.1111/j.1478-3231.2005.01022.x. ISSN 1478-3223. PMID 15698397.
- ↑ Pio, Luca; O'Neill, Allison F.; Woodley, Helen; Murphy, Andrew J.; Tiao, Gregory; Franchi-Abella, Stefanie; Fresneau, Brice; Watanabe, Kenichiro; Alaggio, Rita; Lopez-Terrada, Dolores; Hiyama, Eiso; Branchereau, Sophie (2025-05-22). "Hepatoblastoma". Nature Reviews. Disease Primers. 11 (1): 36. doi:10.1038/s41572-025-00620-7. ISSN 2056-676X. PMID 40404742.
- ↑ Amin, Nisar; Anwar, Javaria; Sulaiman, Abdullahi; Naumova, Nadia Nikolaeva; Anwar, Nadeem (2025-07-02). "Hepatocellular Carcinoma: A Comprehensive Review". Diseases. 13 (7): 207. doi:10.3390/diseases13070207. ISSN 2079-9721. PMC 12293809. PMID 40709997.
- ↑ Jha, Suman K.; Vaqar, Sarosh (2026), "Hereditary Elliptocytosis", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32966004, retrieved 2026-08-21
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- ↑ Althubity, Ayman A. (2026). "Homocystinuria: Advances in metabolic and molecular therapies targeting homocysteine pathways (Review)". Molecular Medicine Reports. 33 (1): 1–13. doi:10.3892/mmr.2025.13745. ISSN 1791-3004. PMC 12612801. PMID 41235668.
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- ↑ Gomułka, Krzysztof; Radzik-Zając, Joanna; Zaleska-Dorobisz, Urszula; Panaszek, Bernard (2017). "Horton's disease: still an important medical problem in elderly patients: a review and case report". Postepy Dermatologii I Alergologii. 34 (5): 510–513. doi:10.5114/ada.2017.71124. ISSN 1642-395X. PMC 5831291. PMID 29507571.
- ↑ Jacob, Joanne S.; Tschen, Jaime (2020-09-23). "Hot Tub-Associated Pseudomonas Folliculitis: A Case Report and Review of Host Risk Factors". Cureus. 12 (9) e10623. doi:10.7759/cureus.10623. ISSN 2168-8184. PMC 7584313. PMID 33123436.
- ↑ Koleva, Miroslava; De Jesus, Orlando (2026), "Hydrocephalus", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32809710, retrieved 2026-08-22
- ↑ Ismail, K. M.; Martin, W. L.; Ghosh, S.; Whittle, M. J.; Kilby, M. D. (2001). "Etiology and outcome of hydrops fetalis". The Journal of Maternal-Fetal Medicine. 10 (3): 175–181. doi:10.1080/714904328. ISSN 1057-0802. PMID 11444786.
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