PedAM

Pediatric Disease Annotations & Medicines


	malabsorption syndrome

Disease ID	1742
Disease	malabsorption syndrome
Definition	Malabsorption: decreased absorption of fat and other nutrients caused by liver, biliary, pancreatic or intestinal disease. The 72-hour fecal fat determination is the best single test for mal- absorption.
Synonym	gastrointestinal absorption disorder intest malabsorption nos intestinal malabsorption intestinal malabsorption (disorder) intestinal malabsorption nos intestinal malabsorption nos (disorder) intestinal malabsorption, nos malabsorption malabsorption syndrome (disorder) malabsorption syndrome nos malabsorption syndrome nos (disorder) malabsorption syndrome, nos malabsorption syndromes malabsorption syndromes [disease/finding] malabsorption, nos syndrome malabsorption syndrome, malabsorption syndromes, malabsorption unspecified intestinal malabsorption
DOID	DOID:8477
UMLS	C0024523
MeSH	D008286
SNOMED-CT	SNOMEDCT_US_2016_09_01:197476001;SNOMEDCT_US_2016_09_01:32230006
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:105) C0011991 \| diarrhea \| 26 C0017178 \| gastrointestinal disease \| 15 C0021831 \| intestinal disease \| 15 C0007570 \| celiac disease \| 15 C0021831 \| intestinal diseases \| 12 C0162429 \| malnutrition \| 12 C0017178 \| gastrointestinal diseases \| 12 C0038238 \| steatorrhea \| 11 C0030293 \| pancreatic insufficiency \| 11 C0002871 \| anemia \| 9 C0011991 \| diarrhoea \| 8 C0010674 \| cystic fibrosis \| 8 C0017152 \| gastritis \| 6 C0029456 \| osteoporosis \| 6 C0033687 \| proteinuria \| 6 C0032827 \| k deficiency \| 6 C0022104 \| irritable bowel syndrome \| 4 C0017536 \| giardiasis \| 4 C0022104 \| irritable bowel \| 4 C0021831 \| enteropathy \| 4 C0020502 \| hyperparathyroidism \| 4 C0017154 \| atrophic gastritis \| 4 C0002871 \| anaemia \| 3 C0267963 \| exocrine pancreatic insufficiency \| 3 C0036992 \| short bowel syndrome \| 3 C0021390 \| inflammatory bowel disease \| 3 C0042870 \| vitamin d defic \| 3 C0042870 \| vitamin d deficiency \| 3 C0002888 \| megaloblastic anemia \| 3 C0162316 \| iron deficiency anemia \| 3 C0042847 \| vitamin b12 defic \| 3 C0020676 \| hypothyroidism \| 3 C0008370 \| cholestasis \| 2 C0017178 \| gastrointestinal disorder \| 2 C1510471 \| vitamin deficiency \| 2 C0162429 \| malnourished \| 2 C0007570 \| coeliac disease \| 2 C0036421 \| systemic sclerosis \| 2 C0178238 \| intestinal infection \| 2 C0010346 \| crohn's disease \| 2 C0042847 \| vitamin b12 deficiency \| 2 C0038238 \| steatorrhoea \| 2 C0017178 \| gastrointestinal disorders \| 2 C0023890 \| cirrhosis \| 2 C0178238 \| intestinal infections \| 2 C0006625 \| cachexia \| 2 C0020503 \| secondary hyperparathyroidism \| 2 C0020541 \| portal hypertension \| 1 C0162429 \| nutritional deficiency \| 1 C0008445 \| chondrodysplasia punctata \| 1 C0020597 \| hypobetalipoproteinemia \| 1 C0017154 \| chronic atrophic gastritis \| 1 C0878544 \| cardiomyopathy \| 1 C0020538 \| hypertension \| 1 C0042875 \| vitamin e deficiency \| 1 C0022951 \| lactose intolerance \| 1 C0020626 \| hypoparathyroidism \| 1 C0023895 \| liver diseases \| 1 C0038362 \| stomatitis \| 1 C0153425 \| small intestine ca \| 1 C0022661 \| end-stage renal disease \| 1 C0275911 \| intestinal tuberculosis \| 1 C0009451 \| communicating hydrocephalus \| 1 C0026846 \| muscle wasting \| 1 C0346976 \| metastatic pancreatic cancer \| 1 C0598608 \| hyperhomocysteinaemia \| 1 C0033680 \| protein-losing enteropathy \| 1 C0007115 \| thyroid ca \| 1 C0035579 \| rickets \| 1 C0018801 \| heart failure \| 1 C0041296 \| tuberculosis \| 1 C0152020 \| gastric stasis \| 1 C0040028 \| essential thrombocythemia \| 1 C0039841 \| thiamine deficiency \| 1 C0004623 \| bacterial infection \| 1 C0235974 \| pancreatic cancer \| 1 C0013473 \| eating disorders \| 1 C0079840 \| milk allergy \| 1 C0030783 \| pellagra \| 1 C0023895 \| liver disease \| 1 C0036202 \| sarcoidosis \| 1 C0038363 \| aphthous stomatitis \| 1 C0007115 \| thyroid cancer \| 1 C0002892 \| pernicious anaemia \| 1 C0085576 \| microcytic anemia \| 1 C0008311 \| cholangitis \| 1 C0028754 \| obesity \| 1 C0010418 \| cryptosporidiosis \| 1 C0020437 \| hypercalcaemia \| 1 C0022658 \| nephropathy \| 1 C0013473 \| eating disorder \| 1 C0020255 \| hydrocephalus \| 1 C0022658 \| renal disease \| 1 C0311273 \| ascending cholangitis \| 1 C0021831 \| bowel disease \| 1 C0029442 \| osteomalacia \| 1 C0023801 \| lipomatosis \| 1 C0004623 \| bacterial infections \| 1 C1510471 \| vitamin deficiencies \| 1 C0238463 \| papillary thyroid cancer \| 1 C0024299 \| lymphoma \| 1 C0162316 \| iron deficiency anaemia \| 1 C0162429 \| undernutrition \| 1 C0836924 \| thrombocythemia \| 1 C0038054 \| tropical sprue \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) SLC46A1 \| 113235 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1742
Disease	malabsorption syndrome
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:88) HP:0002014 \| Diarrhea \| 26 HP:0001824 \| Weight loss \| 16 HP:0002608 \| Celiac disease \| 15 HP:0001903 \| Anemia \| 12 HP:0004395 \| Malnutrition \| 12 HP:0002570 \| Steatorrhea \| 11 HP:0002028 \| Chronic diarrhea \| 10 HP:0000093 \| Proteinuria \| 6 HP:0000939 \| Osteoporosis \| 6 HP:0005263 \| Gastritis \| 6 HP:0002027 \| Abdominal pain \| 5 HP:0011892 \| Vitamin K deficiency \| 5 HP:0001508 \| Weight faltering \| 4 HP:0000843 \| Hyperparathyroidism \| 4 HP:0012432 \| Chronic fatigue \| 4 HP:0012378 \| Fatigue \| 4 HP:0002242 \| Enteropathy \| 4 HP:0011473 \| Villous atrophy \| 4 HP:0003159 \| Hyperoxaluria \| 3 HP:0100512 \| Vitamin D deficiency \| 3 HP:0001738 \| Exocrine pancreatic insufficiency \| 3 HP:0001891 \| Iron-deficiency anemia \| 3 HP:0000821 \| Underactive thyroid \| 3 HP:0001889 \| Megaloblastic anemia \| 3 HP:0001510 \| Growth deficiency \| 3 HP:0004326 \| Cachexia \| 2 HP:0003270 \| Distended abdomen \| 2 HP:0002901 \| Hypocalcemia \| 2 HP:0002015 \| Swallowing difficulty \| 2 HP:0100502 \| Vitamin B12 deficiency \| 2 HP:0012595 \| Mild proteinuria \| 2 HP:0001394 \| Hepatic cirrhosis \| 2 HP:0012531 \| Pain \| 2 HP:0000867 \| Secondary hyperparathyroidism \| 2 HP:0100280 \| Morbus Crohn \| 2 HP:0001548 \| Overgrowth \| 2 HP:0000938 \| Decreased bone mineral density \| 2 HP:0001396 \| Cholestasis \| 2 HP:0002459 \| Dysautonomia \| 1 HP:0001397 \| Hepatic steatosis \| 1 HP:0002960 \| Autoimmune condition \| 1 HP:0001336 \| Myoclonic jerks \| 1 HP:0003563 \| Hypobetalipoproteinemia \| 1 HP:0011967 \| Hypocupremia \| 1 HP:0000822 \| Hypertension \| 1 HP:0002749 \| Osteomalacia \| 1 HP:0002665 \| Lymphoma \| 1 HP:0002748 \| Rickets \| 1 HP:0040216 \| Hypoinsulinemia \| 1 HP:0002917 \| Low blood magnesium levels \| 1 HP:0002018 \| Nausea \| 1 HP:0003774 \| End-stage renal failure \| 1 HP:0002243 \| Protein-losing enteropathy \| 1 HP:0003146 \| Decreased circulating cholesterol level \| 1 HP:0001541 \| Ascites \| 1 HP:0000238 \| Nonsyndromal hydrocephalus \| 1 HP:0001409 \| Portal hypertension \| 1 HP:0100327 \| Cow milk allergy \| 1 HP:0011458 \| Abdominal symptom \| 1 HP:0002582 \| Chronic atrophic gastritis \| 1 HP:0010280 \| Stomatitis \| 1 HP:0000112 \| Nephropathy \| 1 HP:0003073 \| Hypoalbuminaemia \| 1 HP:0000159 \| Lip abnormality \| 1 HP:0001635 \| Congestive heart failure \| 1 HP:0011107 \| Recurrent aphthous stomatitis \| 1 HP:0002718 \| Recurrent pyogenic infections \| 1 HP:0001945 \| Fever \| 1 HP:0100513 \| Vitamin E deficiency \| 1 HP:0005231 \| Chronic gastritis \| 1 HP:0003202 \| Neurogenic muscle atrophy, especially in the lower limbs \| 1 HP:0002894 \| Neoplasia of the pancreas \| 1 HP:0004322 \| Stature below 3rd percentile \| 1 HP:0004789 \| Lactose intolerance \| 1 HP:0000829 \| Hypoparathyroidism \| 1 HP:0030151 \| Cholangitis \| 1 HP:0001513 \| Obesity \| 1 HP:0001638 \| Cardiomyopathy \| 1 HP:0001334 \| Communicating hydrocephalus \| 1 HP:0003072 \| Hypercalcemia \| 1 HP:0002611 \| Cholestatic liver disease \| 1 HP:0012393 \| Allergy \| 1 HP:0002958 \| Immune dysregulation \| 1 HP:0002150 \| Hypercalcinuria \| 1 HP:0001399 \| Liver failure \| 1 HP:0002593 \| Intestinal lymphangiectasia \| 1 HP:0001935 \| Microcytic anemia \| 1 HP:0002514 \| Intracranial calcifications \| 1

Disease ID	1742
Disease	malabsorption syndrome
Manually Symptom	(Waiting for update.)
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:26) C0011991 \| diarrhea \| 26 C0162429 \| malnutrition \| 12 C0021831 \| intestinal diseases \| 12 C0029456 \| osteoporosis \| 6 C0017536 \| giardiasis \| 4 C0020502 \| hyperparathyroidism \| 4 C0042880 \| vitamin k deficiency \| 4 C0015544 \| failure to thrive \| 4 C0021831 \| enteropathy \| 4 C0042870 \| vitamin d deficiency \| 3 C1510471 \| vitamin deficiency \| 2 C0020598 \| hypocalcemia \| 2 C0042847 \| vitamin b12 deficiency \| 2 C0020503 \| secondary hyperparathyroidism \| 2 C0006625 \| cachexia \| 2 C1510471 \| vitamin deficiencies \| 1 C0008445 \| chondrodysplasia punctata \| 1 C0005944 \| metabolic bone disease \| 1 C2004435 \| intestinal ischemia \| 1 C0035579 \| rickets \| 1 C0426768 \| o sign \| 1 C0860204 \| cholestatic liver disease \| 1 C0235950 \| zinc deficiency \| 1 C0029442 \| osteomalacia \| 1 C0042875 \| vitamin e deficiency \| 1 C0268070 \| copper deficiency \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Chemical(Total Drugs:0)
(Waiting for update.)

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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