Digestive Diseases | Page 2

252 diseases found in 3 pages

F Diseases

Fanconi Bickel syndrome Feingold syndrome Fraser syndrome Froster-Huch syndrome Fryns syndrome

G Diseases

Galactokinase deficiency Galactose epimerase deficiency Gardner syndrome Gastrocutaneous syndrome Gastrointestinal Stromal Tumors Gastroschisis Geroderma osteodysplastica Glucose-galactose malabsorption Glycogen storage disease type 1A Glycogen storage disease type 1B Glycogen storage disease type 3 Glycogen storage disease type 6 Goblet cell carcinoid Goldberg-Shprintzen megacolon syndrome GRACILE syndrome

H Diseases

Hemochromatosis type 2 Hemochromatosis type 3 Hemochromatosis type 4 Hepatic encephalopathy Hepatic veno-occlusive disease Hepatic venoocclusive disease with immunodeficiency Hepatoblastoma Hereditary diffuse gastric cancer Hereditary folate malabsorption Hereditary fructose intolerance Hereditary hemorrhagic telangiectasia Hereditary hemorrhagic telangiectasia type 2 Hereditary hemorrhagic telangiectasia type 3 Hereditary hemorrhagic telangiectasia type 4 Hereditary pancreatitis Hirschsprung disease type d brachydactyly Hirschsprung's disease Hyperbilirubinemia transient familial neonatal

I Diseases

Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis Idiopathic achalasia Imerslund-Grasbeck syndrome Immunodysregulation, polyendocrinopathy and enteropathy X-linked Infantile liver failure syndrome 1 Infantile onset spinocerebellar ataxia Intestinal atresia multiple Intrahepatic cholestasis of pregnancy

J Diseases

Jejunal atresia Johanson-Blizzard syndrome Juvenile polyposis syndrome

K Diseases

Kabuki syndrome Kernicterus Klatskin tumor

L Diseases

Limb-body wall complex LRBA deficiency Lucey-Driscoll syndrome Lynch syndrome

M Diseases

Malakoplakia Mallory-Weiss syndrome Meckel syndrome Megacystis microcolon intestinal hypoperistalsis syndrome Megaduodenum and/or megacystis Menetrier disease Mental retardation skeletal dysplasia abducens palsy Microgastria limb reduction defect Microphthalmia syndromic 9 Microphthalmia with linear skin defects syndrome Microvillus inclusion disease Mitochondrial neurogastrointestinal encephalopathy syndrome MOGS-CDG (CDG-IIb) MPI-CDG (CDG-Ib) MPV17-related hepatocerebral mitochondrial DNA depletion syndrome Muir-Torre syndrome Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Multisystemic smooth muscle dysfunction syndrome MURCS association

N Diseases

Necrotizing enterocolitis Neonatal adrenoleukodystrophy Neonatal hemochromatosis Nodular regenerative hyperplasia

O Diseases

Occipital horn syndrome Omphalocele cleft palate syndrome lethal Omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects complex Omphalomesenteric cyst

P Diseases

Pallister-Hall syndrome Pallister-Killian mosaic syndrome Pancreatic adenoma Pancreatic cancer Pearson syndrome Pediatric Crohn's disease Pediatric ulcerative colitis Pentalogy of Cantrell Peutz-Jeghers syndrome PGM1-CDG Plummer Vinson syndrome PMM2-CDG (CDG-Ia) Polycystic liver disease Primary biliary cholangitis Primary intestinal lymphangiectasia

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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