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Human Phenotype Ontology (HPO)

verified

data/human-phenotype-ontology

Standardised vocabulary of phenotypic abnormalities seen in human disease, widely used in rare-disease diagnostics.

A human confirmed this record against its sources within the last 12 months.

record
Category
Data & Standards
Subcategory
ontology
License
NOASSERTION(unknown)
Status
active
Maturity
deployed
Organization
unknown
Country
unknown
Documentation
unknown
Tags
ontology · phenotype · rare-disease
Regulatory
unknown
related
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    Unified disease ontology merging terminology from OMIM, Orphanet, DO, and other sources into a single hierarchy.

built by · 6

Top contributors by commit count, from the project’s public repository. Avatars are served by their origin, not stored here. To be removed from this list, open an issue.

similar by tags

Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.

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sources
  1. api.github.com/repos/obophenotype/human-phenotype-ontology
    retrieved 2026-08-04 · via github-api

    Last push 2026-08-02. GitHub reports NOASSERTION and the LICENSE file only refers readers to the HPO website for licence terms, so no SPDX identifier is recorded.

Verified 2026-08-04 by gh:judegomila. Correct this record →

machine-readable

/v1/entries/19.json→ .entries["human-phenotype-ontology"]

Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.