Human Gene Set: HP_APLASIA_OF_THE_UTERUS


Standard name HP_APLASIA_OF_THE_UTERUS
Systematic name M34570
Brief description Aplasia of the uterus
Full description or abstract A congenital defect characterized by absence of the uterus. Aplasia refers to the failure of an organ to develop during embryonic growth and development due to the absence of primordial tissue. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000151
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000151
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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
Dataset references  
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GTEx compendium
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NCI-60 cell lines (National Cancer Institute)
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Version history 2025.1.Hs: Updated to HPO Release 2025-05-06.

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