Malabsorption
Symptom Information:
Symptom ID: | HPO:0002024 | ||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |