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A Python package to work with the HPO Ontology

Project description

A Python library to work with, analyze, filter and inspect the Human Phenotype Ontology

Visit the PyHPO Documentation for a more detailed overview of all the functionality.

Main features

It allows working on individual terms HPOTerm, a set of terms HPOSet and the full Ontology.

Internally the ontology is represented as a branched linked list, every term contains pointers to its parent and child terms. This allows fast tree traversal functioanlity.

The library is helpful for discovery of novel gene-disease associations and GWAS data analysis studies. At the same time, it can be used for oragnize clinical information of patients in research or diagnostic settings.

It provides an interface to create Pandas Dataframe from its data, allowing integration in already existing data anlysis tools.


An individual HPOTerm contains all info about itself as well as pointers to its parents and its children. You can access its information-content, calculate similarity scores to other terms, find the shortest or longes connection between two terms. List all associated genes or diseases, etc.


An HPOSet can be used to represent e.g. a patient’s clinical information. It allows some basic filtering and comparisons to other HPOSet s.


The Ontology represents all HPO terms and their connections and associations. It also contains pointers to associated genes and disease.

Installation / Setup

The easiest way to install PyHPO is via pip

pip install pyhpo


For a detailed description of how to use PyHPO, visit the PyHPO Documentation.

Getting started

from pyhpo.ontology import Ontology

# initilize the Ontology (you can specify config parameters if needed here)
ontology = Ontology()

# Iterate through all HPO terms
for term in ontology:
    # do something, e.g.

There are multiple ways to retrieve a single term out of an ontology:

# Retrieve a term via its HPO-ID
term = ontology.get_hpo_object('HP:0002650')

# ...or via the Integer representation of the ID
term = ontology.get_hpo_object(2650)

# ...or via shortcut
term = ontology[2650]

# ...or by term name
term = ontology.get_hpo_object('Scoliosis')

You can also do substring search on term names and synonyms:

# returns an Iterator over all matches
for term in'Abn'):

Find the shortest path between two terms:

    'Abnormality of the nervous system',

Working with terms

# check the relationship of two terms

# get the information content for OMIM diseases

# ...or for genes

# compare two terms
term.similarity_score(term2, method='resnik', kind='gene')

Working with sets

# Create a clinical information set of HPO Terms
clinical_info = pyhpo.HPOSet([

# Extract only child nodes and leave out all parent terms
children = clinical_info.child_nodes()

# Remove HPO modifier terms
new_ci = clinical_info.remove_modifier()

# Calculate the similarity of two Sets
sim_score = clinical_info.similarity(other_set)


PyHPO includes some basic statics method for gene, disease and HPO-Term enrichment analysis.

# Let's say you have a patient with a couple of symptoms and
# you want to find out the most likely affected genes
# or most likely diseases

from pyhpo import stats
from pyhpo.ontology import Ontology
from pyhpo.set import HPOSet, BasicHPOSet
_ = Ontology()

hpo_terms = [
    'Decreased circulating antibody level',
    'Abnormal immunoglobulin level',
    'Abnormality of B cell physiology',
    'Abnormal lymphocyte physiology',
    'Abnormality of humoral immunity',
    'Increased circulating IgG level',
    'Abnormal lymphocyte count'

# you can either use a HPOSet for this
hposet = HPOSet.from_queries(hpo_terms)

# or just a plain list of HPO Terms
hposet = [Ontology.match(q) for q in hpo_terms]

# Initialize an Enrichment model for genes
gene_model = stats.EnrichmentModel('gene')

# You can also do enrichment for diseases
disease_model = stats.EnrichmentModel('omim')

# Calculate the Hypergeometric distribution test enrichment
gene_results = gene_model.enrichment(
disease_results = disease_model.enrichment(

# and print the Top-10 results
for x in gene_results[0:10]:
for x in disease_results[0:10]:

and many more examples in the PyHPO Documentation


Yes, please do so. I would appreciate any help, suggestions for improvement or other feedback. Just create a pull-request or open an issue.


PyHPO is released under the MIT license.

PyHPO is using the Human Phenotype Ontology. Find out more at

Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, Julius O B Jacobsen, et al. Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources. Nucleic Acids Research. (2018) doi: 10.1093/nar/gky1105

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