Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Human Phenotype Ontology

Grandparent Node:
All (HP:0000001)

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Parent Node:
Phenotypic abnormality (HP:0000118)

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..Starting node
..Abnormality of the digestive system (HP:0025031)

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Term ID:	25031
Name:	Abnormality of the digestive system
Synonym:
Definition:
Comments:
Reference:	HP:0025031
Genes and Diseases:	There are 703 terms for your input, too many to show detail here. Please try its child terms.
Child Nodes:
........Abnormality of abdomen morphology (HP:0001438) ................... HP:0001541 Ascites ................... HP:0003271 Visceromegaly ................... HP:0005217 Duplication of internal organs ................... HP:0025181 Abdominal aseptic abscess ................... HP:0031500 Abdominal mass ................... HP:0031501 Pelvic mass ................... HP:0031607 Pelvic organ prolapse
........Abnormality of the abdominal organs (HP:0002012) ................... HP:0001392 Abnormality of the liver ................... HP:0001732 Abnormality of the pancreas ................... HP:0001743 Abnormality of the spleen ................... HP:0002585 Abnormality of the peritoneum ................... HP:0011620 Abnormality of abdominal situs ................... HP:0100016 Abnormality of mesentery morphology
........Abnormality of the abdominal wall (HP:0004298) ................... HP:0001551 Abnormality of the umbilicus ................... HP:0004392 Prune belly ................... HP:0010866 Abdominal wall defect ................... HP:0010991 Abnormality of the abdominal musculature ................... HP:0100548 Exstrophy
........Abnormality of the gastrointestinal tract (HP:0011024) ................... HP:0007378 Neoplasm of the gastrointestinal tract ................... HP:0012718 Morphological abnormality of the gastrointestinal tract ................... HP:0012719 Functional abnormality of the gastrointestinal tract
........Abnormality of digestive system physiology (HP:0025032) ................... HP:0011458 Abdominal symptom ................... HP:0012700 Abnormal large intestine physiology ................... HP:0012719 Functional abnormality of the gastrointestinal tract ................... HP:0025155 Abnormality of hepatobiliary system physiology ................... HP:0025156 Dependency on intravenous nutrition
........Abnormality of digestive system morphology (HP:0025033) ................... HP:0012718 Morphological abnormality of the gastrointestinal tract ................... HP:0031685 Abnormal stool composition
Sister Nodes:
..Abnormal cellular phenotype (HP:0025354)
..Abnormality of blood and blood-forming tissues (HP:0001871)
..Abnormality of connective tissue (HP:0003549)
..Abnormality of head or neck (HP:0000152)
..Abnormality of limbs (HP:0040064)
..Abnormality of metabolism/homeostasis (HP:0001939)
..Abnormality of prenatal development or birth (HP:0001197)
..Abnormality of the breast (HP:0000769)
..Abnormality of the cardiovascular system (HP:0001626)
..Abnormality of the ear (HP:0000598)
..Abnormality of the endocrine system (HP:0000818)
..Abnormality of the eye (HP:0000478)
..Abnormality of the genitourinary system (HP:0000119)
..Abnormality of the immune system (HP:0002715)
..Abnormality of the integument (HP:0001574)
..Abnormality of the musculature (HP:0003011)
..Abnormality of the nervous system (HP:0000707)
..Abnormality of the respiratory system (HP:0002086)
..Abnormality of the skeletal system (HP:0000924)
..Abnormality of the thoracic cavity (HP:0045027)
..Abnormality of the voice (HP:0001608)
..Constitutional symptom (HP:0025142)
..Growth abnormality (HP:0001507)
..Neoplasm (HP:0002664)
..obsolete Abnormal test result (HP:0500014)
Genes (0) : Diseases (0) :
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.

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