Human Gene Set: HP_APLASIA_HYPOPLASIA_OF_FACIAL_BONES


Standard name HP_APLASIA_HYPOPLASIA_OF_FACIAL_BONES
Systematic name M46365
Brief description Aplasia/Hypoplasia of facial bones
Full description or abstract A developmental defect characterized by absence or underdevelopment of one or more facial bone. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0034261
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0034261
Filtered by similarity ? (show 1 similar ontology term(s) from the external resource)
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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NCI-60 cell lines (National Cancer Institute)
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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