Human Gene Set: HP_AMYLOIDOSIS


Standard name HP_AMYLOIDOSIS
Systematic name M37745
Brief description Amyloidosis
Full description or abstract The presence of amyloid deposition in one or more tissues. Amyloidosis may be defined as the extracellular deposition of amyloid in one or more sites of the body. [https://orcid.org/0000-0002-0736-9199, PMID:21039326]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0011034
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0011034
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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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Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 35 genes
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Show members (show 35 source identifiers mapped to 35 genes)
Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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