Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/6
From Wikipedia, the free encyclopedia
| WikiProject Missing encyclopedic articles
|
|---|
| Project page - The goal of this project is to ensure that Wikipedia has a corresponding article for every article in every other encyclopedia. Sign in! |
| Weekly focus : Hotlist of topics/A4 Only 276 remain! |
| Hotlist of topics - 71% done |
| 1911 verification - 1.6% |
| General topics - 58.8% done |
| Other Wikipedias: de es fr |
| Biographies - 95.2% done |
| Science topics >40% done |
| Catholic topics - 39.1% done |
| Easton's Bible Dictionary - 23.0% done |
| Gutenberg authors - 33.7% done |
| Literary Encyclopedia - 67.2% done |
| Find-A-Grave - 13.7% done |
| Miscellaneous |
| Many other lists of politicians, albums, films, TV shows and others. |
| Overall progress - 43.7% |
| Spread the word! {{Project missing articles}} |
- Hagemoser Weinstein Bresnick syndrome
- Hailey-Hailey disease
- Hair defect with photosensitivity and mental retardation
- Hairy ears, y-linked
- Hairy ears
- Hairy nose tip
- Hairy palms and soles
- Hajdu-Cheney syndrome
- Halal Setton Wang syndrome
- Halal syndrome
- Hall Riggs mental retardation syndrome
- Hallervorden-Spatz disease
- Hamanishi Ueba Tsuji syndrome
- Hamano Tsukamoto syndrome
- Hamartoma sebaceus of Jadassohn
- Hand and foot deformity flat facies
- Hand foot uterus syndrome
- Hand-Schuller-Christian disease
- Hanhart syndrome
- Hapnes Boman Skeie syndrome
- Hard skin syndrome Parana type
- Harding ataxia
- Harrod Doman Keele syndrome
- Hartsfield Bixler Demyer syndrome
- Hashimoto struma
- Hashimoto-Pritzker syndrome
- Haspeslagh Fryns Muelenaere syndrome
- Hay Wells syndrome recessive type
- Hay-Wells syndrome
- Heart aneurysm
- Heart block progressive, familial
- 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
- Hec syndrome
- Hecht Scott syndrome
- Heckenlively syndrome
- Heide syndrome
- Helmerhorst Heaton Crossen syndrome
- HEM dysplasia
- Hemangioblastoma
- Hemangioma thrombocytopenia syndrome
- Hemangioma, capillary infantile
- Hemangiomatosis, familial pulmonary capillary
- Hemeralopia, congenital essential
- Hemeralopia, familial
- Hemi 3 syndrome
- Hemifacial atrophy agenesis of the caudate nucleus
- Hemifacial atrophy progressive
- Hemifacial hyperplasia strabismus
- Hemihypertrophy in context of NF
- Hemihypertrophy intestinal web corneal opacity
- Hemimegalencephaly
- Hemiplegic migraine, familial
- Hemoglobin C disease
- Hemoglobin E disease
- Hemoglobin SC disease
- Hemolytic anemia lethal genital anomalies
- Hemophagocytic lymphohistiocytosis
- Hemophagocytic reticulosis
- Hemophilic arthropathy
- Hemorragic fever with renal syndrome
- Hemorrhagic proctocolitis
- Hemorrhagic thrombocythemia
- Hemorrhagiparous thrombocytic dystrophy
- Hennekam Beemer syndrome
- Hennekam Koss de Geest syndrome
- Hennekam syndrome
- Hennekam Van der Horst syndrome
- Hepadnovirus D
- Heparane sulfamidase deficiency
- Hepatic cystic hamartoma
- Hepatic ductular hypoplasia
- Hepatic fibrosis renal cysts mental retardation
- Hepatic fibrosis
- Hepatic venoocclusive disease
- Hepatic veno-occlusive disease
- Hepatorenal tyrosinemia
- Hereditary carnitine deficiency myopathy
- Hereditary carnitine deficiency syndrome
- Hereditary carnitine deficiency
- Hereditary hyperuricemia
- Hereditary macrothrombocytopenia
- Hereditary methemoglobinemia, recessive
- Hereditary myopathy with intranuclear filamentous
- Hereditary nodular heterotopia
- 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 spherocytic hemolytic anemia
- Hereditary type 1 neuropathy
- Hereditary type 2 neuropathy
- Hernandez Aguire Negrete syndrome
- Herpes encephalitis
- Herpes virus antenatal infection
- Herpesvirus simiae B virus
- Herpetic embryopathy
- Herrmann Opitz arthrogryposis syndrome
- Herrmann Opitz craniosynostosis
- Hers disease
- Hersh Podruch Weisskopk syndrome
- Heterotaxia (generic term)
- Heterotaxia autosomal dominant type
- Heterotaxy with polysplenia or asplenia
- Heterotaxy, visceral, X-linked
- Hexosaminidases A and B deficiency
- HHH syndrome
- Hibernian fever, familial
- Hidradenitis suppurativa familial
- 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 luxation
- Hip subluxation
- Hipo syndrome
- 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
- Histidinemia
- Histidinuria renal tubular defect
- Histiocytosis, Non-Langerhans-Cell
- Hittner Hirsch Kreh syndrome
- Hm syndrome
- HMG CoA lyase deficiency
- HMG CoA synthetase deficiency
- Hoepffner Dreyer Reimers syndrome
- Hollow visceral myopathy
- Holmes Benacerraf syndrome
- Holmes Borden syndrome
- Holmes Collins syndrome
- Holmes Gang syndrome
- Holoacardius amorphus
- Holoprosencephaly caudal dysgenesis
- Holoprosencephaly deletion 2p
- Holoprosencephaly ectrodactyly cleft lip palate
- Holoprosencephaly radial heart renal anomalies
- Holt-Oram syndrome
- Holzgreve Wagner Rehder syndrome
- 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
- Homologous wasting disease
- Homozygous hypobetalipoproteinemia
- Hoon Hall syndrome
- Hordnes Engebretsen Knudtson syndrome
- Horn Kolb syndrome
- Hornova Dlurosova syndrome
- Horton disease, juvenile
- Horton disease
- Houlston Ironton Temple syndrome
- Howard Young syndrome
- Hoyeraal Hreidarsson syndrome
- Hoyeraal syndrome
- Human granulocytic ehrlichiosis
- Human monocytic ehrlichiosis
- Humero spinal dysostosis congenital heart disease
- Humeroradial synostosis
- Humeroradioulnar synostosis
- Humerus trochlea aplasia of
- Hunter Carpenter Mc donald syndrome
- Hunter Jurenka Thompson syndrome
- Hunter Macpherson syndrome
- Hunter Mcalpine syndrome
- Hunter Mcdonald syndrome
- Hunter Rudd Hoffmann syndrome
- Huriez scleroatrophic syndrome
- Hurst Hallam Hockey syndrome
- Hutteroth Spranger syndrome
- Hyalinosis systemic short stature
- Hyaloideoretinal degeneration of wagner
- Hyde Forster Mccarthy Berry syndrome
- 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
- Hydrocephaly corpus callosum agenesis diaphragmatic hernia
- Hydrocephaly low insertion umbilicus
- Hydrocephaly tall stature joint laxity
- Hydrolethalus syndrome
- Hydronephrosis peculiar facial expression
- Hydrops ectrodactyly syndactyly
- Hydrops fetalis anemia immune disorder absent thumb
- Hydroxycarboxylic aciduria
- Hydroxymethylglutaricaciduria
- Hygroma cervical
- Hyper IgE
- Hyper IgM syndrome
- Hyperadrenalism
- Hyperaldosteronism familial type 2
- Hyperaldosteronism, familial type 1
- Hyperbilirubinemia transient familial neonatal
- Hyperbilirubinemia type 1
- Hyperbilirubinemia type 2
- Hypercalcemia, familial benign type 1
- Hypercalcemia, familial benign type 2
- Hypercalcemia, familial benign type 3
- Hypercalcemia, familial benign
- Hypercalcinuria idiopathic
- Hypercalcinuria macular coloboma
- Hypercalcinuria
- Hypercementosis
- Hypercholesterolemia due to arg3500 mutation of Apo B-100
- Hypercholesterolemia due to LDL receptor deficiency
- Hyperferritinemia, hereditary, with congenital cataracts
- Hypergeusia
- Hyperglycerolemia
- Hyperglycinemia, isolated nonketotic type 1
- Hyperglycinemia, isolated nonketotic type 2
- Hyperglycinemia, isolated nonketotic
- Hypergonadotropic ovarian failure, familial or sporadic
- Hyperhomocysteinemia
- Hyperimidodipeptiduria
- Hyperimmunoglobulin E - reccurrent 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
- Hyperkeratosis lenticularis perstans of Flegel
- Hyperkeratosis lenticularis perstans
- Hyperkeratosis palmoplantar localized acanthokeratolytic
- Hyperkeratosis palmoplantar localized epidermolytic
- Hyperkeratosis palmoplantar with palmar crease hyperkeratosis
- Hyperornithinemia
- Hyperornithinemia-hyperammonemia-homocitrullinuria
- Hyperostosid corticalis deformans juvenilis
- Hyperostosis cortical infantile
- Hyperostosis corticalis generalisata
- Hyperostosis frontalis interna
- Hyperoxaluria type 1
- Hyperoxaluria type 2
- Hyperoxaluria
- Hyperparathyroidism, familial, primary
- Hyperparathyroidism, neonatal severe primary
- Hyperphalangism dysmorphy bronchomalacia
- Hyperphenilalaninemia due to pterin-4-alpha-carbin
- Hyperphenylalalinemia due to dihydropteridine reductase deficiency
- Hyperphenylalaninemia due to 6-pyruvoyltetrahydrop
- Hyperphenylalaninemia due to dehydratase deficiency
- Hyperphenylalaninemia due to GTP cyclohydrolase deficiency
- Hyperphenylalaninemic embryopathy
- Hyperpipecolatemia
- Hyperprolinemia type II
- Hyperprolinemia
- Hyper-reninism
- Hypersomnolence
- Hypertelorism and tetralogy of Fallot
- Hypertelorism hypospadias syndrome
- Hypertensive hyperkalemia, familial
- Hypertensive hypokalemia familial
- Hyperthermia induced defects
- 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 hemangiectasia
- Hypertrophic myocardiopathy
- Hypertrophic osteoarthropathy, primary or idiopathic
- Hypertropic neuropathy of Dejerine-Sottas
- Hypertryptophanemia
- Hypoadrenocorticism hypoparathyroidism moniliasis
- Hypo-alphalipoproteinemia primary
- Hypobetalipoprotéinemia, familial
- Hypobetalipoproteinaemia ataxia hearing loss
- Hypocalcemia, autosomal dominant
- Hypocalcinuric hypercalcemia, familial type 1
- Hypocalcinuric hypercalcemia, familial type 2
- Hypocalcinuric hypercalcemia, familial type 3
- Hypocalcinuric hypercalcemia, familial
- Hypocomplementemic urticarial vasculitis
- Hypodermyasis
- Hypodontia dysplasia of nails
- Hypodontia of incisors and premolars
- Hypofibrinogenemia, familial
- Hypoglycemia with deficiency of glycogen synthetase in the liver
- 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
- Hypogonadotropic hypogonadism syndactyly
- Hypogonadotropic hypogonadism without anosmia, X linked
- Hypogonadotropic hypogonadism-anosmia, X linked
- Hypogonadotropic hypogonadism-anosmia
- Hypohidrotic Ectodermal Dysplasia
- Hypokalemic alkalosis with hypercalcinuria
- Hypokaliemic periodic paralysis type 1
- Hypoketonemic hypoglycemia
- Hypolipoproteinemia
- Hypomagnesemia primary
- Hypomandibular faciocranial dysostosis
- Hypomelanotic disorder
- Hypomelia mullerian duct anomalies
- Hypomentia
- Hypoparathyroidism familial isolated
- Hypoparathyroidism nerve deafness nephrosis
- Hypoparathyroidism short stature mental retardation
- Hypoparathyroidism short stature
- Hypoparathyroidism X linked
- Hypophosphatasia, infantile
- Hypophosphatemic rickets
- Hypopigmentation oculocerebral syndrome Cross type
- Hypopituitarism micropenis cleft lip palate
- Hypopituitarism postaxial polydactyly
- Hypopituitary dwarfism
- Hypoplasia hepatic ductular
- Hypoplasia of the tibia with polydactyly
- Hypoplastic right heart microcephaly
- Hypoplastic thumb mullerian aplasia
- Hypoplastic thumbs hydranencephaly
- Hypoproconvertinemia
- Hyporeninemic hypoaldosteronism
- Hyposmia nasal hypoplasia hypogonadism
- Hypospadias mental retardation Goldblatt type
- Hypotelorism cleft palate hypospadias
- Hypothalamic hamartomas
- Hypothyroidism due to iodide transport defect
- Hypothyroidism postaxial polydactyly mental retardation
- Hypotonic sclerotic muscular dystrophy
- Hypotrichosis mental retardation Lopes type
- Hypotrichosis
- Hypoxanthine guanine phosphoribosyltransferase deficiency
- I cell disease
- IBIDS syndrome
- Ichthyosiform erythroderma corneal involvement deafness
- Ichthyosis alopecia eclabion ectropion mental retardation
- Ichthyosis and male hypogonadism
- Ichthyosis bullosa of Siemens
- Ichthyosis cheek eyebrow syndrome
- Ichthyosis congenita biliary atresia
- Ichthyosis deafness mental retardation skeletal anomaly
- Ichthyosis follicularis atrichia photophobia syndrome
- Ichthyosis hepatosplenomegaly cerebellar degeneration
- Ichthyosis hystrix, Curth Macklin type
- Ichthyosis linearis circumflexa
- Ichthyosis male hypogonadism
- Ichthyosis mental retardation Devriendt type
- Ichthyosis mental retardation dwarfism renal impairment
- Ichthyosis microphthalmos
- Ichthyosis tapered fingers midline groove up
- Ichthyosis, erythrokeratolysis hemalis
- Ichthyosis, keratosis follicularis spinulosa Decalvans
- Ichthyosis, lamellar recessive
- Ichthyosis, Netherton syndrome
- Idaho syndrome
- Idiopathic adult neutropenia
- Idiopathic alveolar hypoventilation syndrome
- Idiopathic congenital nystagmus, dominant, X- linked
- Idiopathic diffuse interstitial fibrosis
- Idiopathic dilatation of the pulmonary artery
- Idiopathic dilation cardiomyopathy
- Idiopathic double athetosis
- Idiopathic edema
- Idiopathic eosinophilic chronic pneumopathy
- Idiopathic facial palsy
- Idiopathic hypereosinophilic syndrome
- Idiopathic infection caused by BCG or atypical mycobacteria
- Idiopathic juvenile osteoporosis
- Idiopathic pulmonary hemosiderosis
- Idiopathic sclerosing mesenteritis
- Iduronate 2-sulfatase deficiency
- IFAP syndrome
- IgA deficiency
- IGDA syndrome
- Illum syndrome
- Illyngophobia
- Ilyina Amoashy Grygory syndrome
- Imaizumi Kuroki syndrome
- Iminoglycinuria
- Immotile cilia syndrome, due to defective radial spokes
- Immotile cilia syndrome, due to excessively long cilia
- Immotile cilia syndrome, Kartagener type
- Immune deficiency, familial variable
- Immune thrombocytopenia
- Immunodeficiency with short limb dwarfism
- Immunodeficiency, microcephaly with normal intelligence
- Imperforate oropharynx costo vetebral anomalies
- Inactive colon
- Inborn amino acid metabolism disorder
- Inborn branched chain aminoaciduria
- Inborn metabolic disorder
- Inborn renal aminoaciduria
- Inborn urea cycle disorder
- Incisors fused
- Inclusion conjunctivitis
- Incontinentia pigmenti type 1
- Incontinentia pigmenti type 2
- Indomethacin antenatal infection
- Infant epilepsy with migrant focal crisis
- Infantile apnea
- Infantile axonal neuropathy
- Infantile convulsions and paroxysmal choreoathetosis, familial
- Infantile digital fibromatosis
- Infantile dysphagia
- Infantile multisystem inflammatory disease
- Infantile myofibromatosis
- Infantile onset spinocerebellar ataxia
- Infantile recurrent chronic multifocal osteomyolitis
- Infantile sialic acid storage disorder
- Infantile spasms broad thumbs
- Infantile striato thalamic degeneration
- Infectious arthritis
- Infectious myocarditis
- Infundibulopelvic stenosis multicystic kidney
- Insensitivity to pain with anhidrosis
- Instability mitotic non disjunction syndrome
- Insulin-resistance type B
- Insulin-resistant acanthosis nigricans, type A
- Intercellular cholesterol esterification disease
- Interferon gamma, receptor 1, deficiency
- Internal carotid agenesis
- Interstitial pneumonia
- Intestinal atresia multiple
- Intestinal lipodystrophy
- Intestinal lymphangiectasia
- Intestinal malrotation facial anomalies familial type
- Intoeing
- Intracranial aneurysms multiple congenital anomaly
- Intracranial arterioveinous malformation
- Intractable singultus
- Intrathoracic kidney vertebral fusion
- Intrauterine growth retardation mandibular malar hypoplasia
- Intrauterine infections
- Intrinsic factor, congenital deficiency of
- Iodine antenatal infection
- Iophobia
- Iridogoniodysgenesis, dominant type
- Iris dysplasia hypertelorism deafness
- Irons Bhan syndrome
- Isaacs Mertens syndrome
- Isaacs syndrome
- Ischiadic hypoplasia renal dysfunction immunodeficiency
- Ischiopatellar dysplasia
- Isosporosiasis
- Isotretinoin embryopathy
- Isthmian coarctation
- Ivemark syndrome
- Ivic Syndrome
- Jadassohn Lewandowsky syndrome
- Jaffer Beighton syndrome
- Jalili syndrome
- Jancar syndrome
- Jankovic Rivera syndrome
- Jansen type metaphyseal chondrodysplasia
- Jansky-Bielschowsky disease
- Jarcho-Levin syndrome
- Jejunal atresia
- Jensen syndrome
- Jequier Kozlowski skeletal dysplasia
- Jervell Lange-Nielsen syndrome
- Jeune syndrome situs inversus
- Jeune syndrome
- Job syndrome
- Johanson Blizzard syndrome
- Johnson Hall Krous syndrome
- Johnston Aarons Schelley syndrome
- Jones Hersh Yusk syndrome
- Jones syndrome
- Jorgenson Lenz syndrome
- Joseph disease
- Joubert syndrome bilateral chorioretinal coloboma
- Juberg Hayward syndrome
- Juberg Marsidi syndrome
- Judge Misch Wright syndrome
- Jung Wolff Back Stahl syndrome
- Juvenile cataract cerebellar atrophy myopathy mental retardation
- Juvenile gastrointestinal polyposis
- Juvenile gout
- Juvenile hyaline fibromatosis
- Juvenile macular degeneration hypotrichosis
- Juvenile muscular atrophy of the distal upper limb
- Juvenile myoclonic epilepsy
- Juvenile nephronophthisis
- Juvenile temporal arteritis
