Malabsorption

Symptom Information:

Symptom ID: HPO:0002024
Synonyms:
Intestinal malabsorption [HPO:0002024]
Intestinal Malabsorption [Orphanet:27360]
Intestinal malabsorption (disorder) [Orphanet:27360]
Malabsorption syndrome (disorder) [Orphanet:27360]
Malabsorption Syndrome [Orphanet:27360]
Intestinal malabsorption [OMIM:Intestinal malabsorption]
Malabsorption [OMIM:Malabsorption]
Malabsorption/chronic diarrhea/steatorrhea [Orphanet:27360]
Malabsorption [Orphanet:27360]
Malabsorption [MedDRA:10025476]
Intestinal malabsorption [MedDRA:10025476]
Malabsorption syndrome [MedDRA:10025476]
Other specified intestinal malabsorption [MedDRA:10025476]
Sprue [MedDRA:10025476]
Sprue NOS [MedDRA:10025476]
Syndrome malabsorption [MedDRA:10025476]
Syndrome sprue-like [MedDRA:10025476]
Unspecified intestinal malabsorption [MedDRA:10025476]
Malabsorption (small intestine) [OMIM:Malabsorption (small intestine)]
Malabsorption syndromes [MedDRA:10025480]
Quality:
Cross references:
Orphanet:27360 "Malabsorption/chronic diarrhea/steatorrhea" [Orphanet:27360]
OMIM: "Intestinal malabsorption" [OMIM:Intestinal malabsorption]
OMIM: "Malabsorption" [OMIM:Malabsorption]
OMIM: "Malabsorption (small intestine)" [OMIM:Malabsorption (small intestine)]
UMLS:C1963165 "Malabsorption" [HPO:0002024]
UMLS:C0024523 "Malabsorption Syndrome" [Orphanet:27360]
Is a (Direct Parents):
Orphanet Functional anomalies of the digestive system
HPO         Abnormality of the intestine
MedDRA Malabsorption conditions
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of the intestine(HPO:0002242)
                   Malabsorption(HPO:0002024)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Malabsorption conditions(MedDRA:10025477)
       Malabsorption(HPO:0002024)
Database Frequency: 142 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2 (OMIM:300310)
AL amyloidosis (Orphanet:85443)
Abetalipoproteinemia (Orphanet:14)
Acquired hypertrichosis lanuginosa (Orphanet:2221)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Aggressive systemic mastocytosis (Orphanet:98850)
Aicardi syndrome (Orphanet:50)
Alpha heavy-chain disease (Orphanet:100025)
Aplasia cutis congenita - intestinal lymphangiectasia (Orphanet:1116)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Aspartylglucosaminuria (Orphanet:93)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal recessive cerebelloparenchymal disorder type 3 (Orphanet:1170)
Baller-Gerold syndrome (Orphanet:1225)
Behçet disease (Orphanet:117)
Benign recurrent intrahepatic cholestasis (Orphanet:65682)
Beta-thalassemia major (Orphanet:231214)
Budd-Chiari syndrome (Orphanet:131)
Cartilage-hair hypoplasia (Orphanet:175)
Celiac disease, epilepsy and cerebral calcification syndrome (Orphanet:1459)
Central nervous system calcification - deafness - tubular acidosis - anemia (Orphanet:3240)
Cerebrotendinous xanthomatosis (Orphanet:909)
Cholestasis - lymphedema (Orphanet:1414)
Cholesteryl ester storage disease (Orphanet:75234)
Choreoacanthocytosis (Orphanet:2388)
Chronic granulomatous disease (Orphanet:379)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Common variable immunodeficiency (Orphanet:1572)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 2 (Orphanet:79303)
Congenital bile acid synthesis defect type 4 (Orphanet:79095)
Congenital lethal erythroderma (Orphanet:1954)
Congenital sucrase-isomaltase deficiency (Orphanet:35122)
Cronkhite-Canada syndrome (Orphanet:2930)
Cutaneous mastocytosis (Orphanet:66646)
Cutaneous photosensitivity - lethal colitis (Orphanet:2881)
Cutis laxa (Orphanet:209)
Cystic fibrosis (Orphanet:586)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Cystinosis (Orphanet:213)
Deafness - small bowel diverticulosis - neuropathy (Orphanet:3217)
Dermatitis herpetiformis (Orphanet:1656)
Desmoid tumor (Orphanet:873)
Diffuse cutaneous mastocytosis (Orphanet:79456)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Disorder of bile acid synthesis (Orphanet:79168)
Dubowitz syndrome (Orphanet:235)
Dyskeratosis congenita (Orphanet:1775)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Epidermolysis bullosa simplex due to plakophilin deficiency (Orphanet:158668)
Erythroderma desquamativum (Orphanet:314)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Floating-Harbor syndrome (Orphanet:2044)
Gaucher disease type 3 (Orphanet:77261)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
HYPERLYSINURIA WITH HYPERAMMONEMIA (OMIM:238750)
Hartnup syndrome (Orphanet:2116)
Hennekam syndrome (Orphanet:2136)
Hereditary central diabetes insipidus (Orphanet:30925)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary nonpolyposis colon cancer (Orphanet:144)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hurler syndrome (Orphanet:93473)
Hyperdibasic aminoaciduria type 1 (Orphanet:1032)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
ICF syndrome (Orphanet:2268)
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 (OMIM:242860)
IMMUNOGLOBULIN A DEFICIENCY 1 (OMIM:137100)
INTRINSIC FACTOR DEFICIENCY (OMIM:261000)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
Intestinal lymphangiectasia (Orphanet:36204)
Isolated agammaglobulinemia (Orphanet:229717)
Johanson-Blizzard syndrome (Orphanet:2315)
Juvenile idiopathic arthritis (Orphanet:92)
Juvenile polyposis syndrome (Orphanet:2929)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
LIG4 syndrome (Orphanet:99812)
Linear IgA dermatosis (Orphanet:46488)
Lyell syndrome (Orphanet:537)
Lysosomal acid lipase deficiency (Orphanet:275761)
MELAS (Orphanet:550)
MITCHELL-RILEY SYNDROME (OMIM:615710)
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) (OMIM:603041)
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) (OMIM:613662)
MPI-CDG (Orphanet:79319)
Majeed syndrome (Orphanet:77297)
Malignant atrophic papulosis (Orphanet:679)
Marshall syndrome with periodic fever (Orphanet:42642)
Maternally-inherited diabetes and deafness (Orphanet:225)
Menkes disease (Orphanet:565)
Microvillous inclusion disease (Orphanet:2290)
Mitochondrial neurogastrointestinal encephalomyopathy (Orphanet:298)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Natal teeth - intestinal pseudoobstruction - patent ductus (Orphanet:1654)
Netherton syndrome (Orphanet:634)
Nijmegen breakage syndrome (Orphanet:647)
Non-polyposis Turcot syndrome (Orphanet:99817)
Obesity due to prohormone convertase I deficiency (Orphanet:71528)
Oculocerebrorenal syndrome (Orphanet:534)
Oculogastrointestinal muscular dystrophy (Orphanet:1876)
Omenn syndrome (Orphanet:39041)
Pachydermoperiostosis (Orphanet:2796)
Pearson syndrome (Orphanet:699)
Polyarteritis nodosa (Orphanet:767)
Primary intestinal lymphangiectasia (Orphanet:90362)
Primary systemic amyloidosis (Orphanet:314701)
Progressive familial intrahepatic cholestasis (Orphanet:172)
Progressive familial intrahepatic cholestasis type 3 (Orphanet:79305)
RAPADILINO syndrome (Orphanet:3021)
Reactive arthritis (Orphanet:29207)
Reticular dysgenesis (Orphanet:33355)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
SAPHO syndrome (Orphanet:793)
SATOYOSHI SYNDROME (OMIM:600705)
Scleroderma (Orphanet:801)
Secondary intestinal lymphangiectasia (Orphanet:90363)
Severe combined immunodeficiency (Orphanet:183660)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
Shwachman-Diamond syndrome (Orphanet:811)
Siegler-Brewer-Carey syndrome (Orphanet:3167)
Stevens-Johnson syndrome (Orphanet:36426)
Sweet syndrome (Orphanet:3243)
Systemic mastocytosis (Orphanet:2467)
Systemic sclerosis (Orphanet:90291)
Waldenström macroglobulinemia (Orphanet:33226)
Whipple disease (Orphanet:3452)
Williams syndrome (Orphanet:904)
Wolfram syndrome (Orphanet:3463)
Wolman disease (Orphanet:75233)
X-linked agammaglobulinemia (Orphanet:47)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
Zellweger syndrome (Orphanet:912)