Human Phenotype
Ontology
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Grandparent Node: Abnormality of the peritoneum (HP:0002585) |
Grandparent Node: Serositis (HP:0045073) |
Parent Node: Peritonitis (HP:0002586) |
..Starting node ..Meconium peritonitis (HP:0030717)
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Term ID: |
30717 |
Name: |
Meconium peritonitis |
Synonym: |
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Definition: |
Peritonitis caused by intrauterine intestinal rupture and spillage of fetal meconium into the fetal peritoneal cavity. Intra-peritoneal meconium usually calcifies, sometimes within 24 hours. Ultrasound findings may include intraabdominal calcifications. |
Comments: |
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Reference: |
HP:0030717 |
Genes and Diseases: | | Child Nodes: | Sister Nodes: |
Genes (1) :CDC45
Diseases (1) :OMIM:617063 |
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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