Human Gene Set: HP_FINGER_APLASIA


Standard name HP_FINGER_APLASIA
Systematic name M37373
Brief description Finger aplasia
Full description or abstract A developmental defect resulting in the presence of fewer than the normal number of fingers (i.e., aplasia of one or more fingers). [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0009380
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0009380
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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 86 genes
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Show members (show 86 source identifiers mapped to 86 genes)
Version history 2024.1.Hs: Renamed from HP_APLASIA_OF_THE_FINGERS. Updated to HPO Release 2024-04-26.

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