Human Gene Set: HP_APLASIA_HYPOPLASIA_OF_THE_RETINA


Standard name HP_APLASIA_HYPOPLASIA_OF_THE_RETINA
Systematic name M37174
Brief description Aplasia/Hypoplasia of the retina
Full description or abstract  
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0008061
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0008061
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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)
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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