Human Gene Set: HP_GONADAL_DYSGENESIS


Standard name HP_GONADAL_DYSGENESIS
Systematic name M34557
Brief description Gonadal dysgenesis
Full description or abstract Gonadal dysgenesis is the name given to any of a multitude of conditions that can cause impaired development of the gonads, i.e., the testes or ovaries, or to the related phenotypic features. The term is to be avoided if possible for new annotations, and more specific terms should be chosen. [PMID:30969708]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000133
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000133
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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
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 38 genes
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Version history 2025.1.Hs: Updated to HPO Release 2025-05-06.

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