OpenLife Sciences

HPO

Human Phenotype Ontology

Standardized vocabulary of phenotypic abnormalities. 16,000+ terms critical for rare disease diagnosis.

phenotypesrare-diseasesgenomics
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Class Hierarchy

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Use Cases

When and where you'd use this ontology in practice.

01

Rare disease differential diagnosis

02

Clinical genomics variant interpretation

03

Patient phenotype-based gene prioritization

04

Newborn screening program data analysis

Details

Maintained By
Monarch Initiative / JAX
License
Open

This licence label has not been independently verified against the licence text. Check the ontology's own site before relying on it.

Category
Life Sciences

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