Human Gene Set: HP_ABNORMAL_INTESTINE_MORPHOLOGY


Standard name HP_ABNORMAL_INTESTINE_MORPHOLOGY
Systematic name M35728
Brief description Abnormal intestine morphology
Full description or abstract An abnormality of the intestine. The closely related term enteropathy is used to refer to any disease of the intestine. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002242
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002242
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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