Human Phenotype Ontology 
Grandparent Node:
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Abnormality of digestive system physiology (HP:0025032)help
Parent Node:
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Abdominal symptom (HP:0011458)help
..Starting node
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Malnutrition (HP:0004395)help
Term ID: 4395
Name: Malnutrition
Synonym: Malnutrition
Definition:
Comments:
Reference: HP:0004395
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbdominal distention (HP:0003270) help
..expandAbdominal pain (HP:0002027) help
..expandAbnormal bowel sounds (HP:0030142) help
..expandAnorexia (HP:0002039) help
..expandConstipation (HP:0002019) help
..expandDiarrhea (HP:0002014) help
..expandFeeding difficulties (HP:0011968) help
..expandNausea and vomiting (HP:0002017) help
..expandPoor appetite (HP:0004396) help
..expandProtein avoidance (HP:0002038) help
..expandScaphoid abdomen (HP:0025063) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0004395HP:0004395Malnutrition0ACTG2 CL E G H72155310Visceral myopathy155310C1835084OMIM12049145102545
HP:0004395HP:0004395Malnutrition0ALDOB CL E G H229229600Hereditary fructosuria229600C0016751OMIM167210417612724
HP:0004395HP:0004395Malnutrition0COL7A1 CL E G H1294226600Recessive dystrophic epidermolysis bullosa226600C0079474OMIM18286912214120120
HP:0004395HP:0004395Malnutrition0COX4I2 CL E G H84701612714Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis612714C2675184OMIM113316232607976
HP:0004395HP:0004395Malnutrition0LIPA CL E G H398875233ORPHA1962466617613497
HP:0004395HP:0004395Malnutrition0MYO5B CL E G H4645251850Congenital microvillous atrophy251850C0341306OMIM1814197603606540
HP:0004395HP:0004395Malnutrition0POLG CL E G H5428603041Mitochondrial DNA depletion syndrome 1 (MNGIE type)603041C0872218OMIM130011969179174763
HP:0004395HP:0004395Malnutrition0POLG CL E G H5428613662Mitochondrial DNA depletion syndrome 4B, MNGIE type613662C3150914OMIM130011969179174763
HP:0004395HP:0004395Malnutrition0SAA1 CL E G H628885445ORPHA132410513104750
HP:0004395HP:0004395Malnutrition0SAR1B CL E G H51128246700Chylomicron retention disease246700C0795956OMIM1163710535607690
HP:0004395HP:0004395Malnutrition0SLC7A7 CL E G H9056222700Lysinuric protein intolerance222700C0268647OMIM16725211065603593
HP:0004395HP:0004395Malnutrition0TYMP CL E G H1890603041Mitochondrial DNA depletion syndrome 1 (MNGIE type)603041C0872218OMIM1953813148131222
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (11) :ACTG2 ALDOB COL7A1 COX4I2 LIPA MYO5B POLG SAA1 SAR1B SLC7A7 TYMP

Diseases (11) :155310 229600 226600 612714 75233 251850 603041 613662 85445 246700 222700
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.