Human Gene Set: HP_ABNORMAL_HELIX_MORPHOLOGY


Standard name HP_ABNORMAL_HELIX_MORPHOLOGY
Systematic name M37750
Brief description Abnormal helix morphology
Full description or abstract An abnormality of the helix. The helix is the outer rim of the ear that extends from the insertion of the ear on the scalp (root) to the termination of the cartilage at the earlobe. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0011039
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0011039
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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
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Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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