monarch-database

Overview

The Monarch Initiative integrates disease-phenotype-gene relationships from 30+ biomedical databases (OMIM, Orphanet, ClinVar, MGI, ZFIN, Reactome) into a unified knowledge graph. The REST API at https://api.monarchinitiative.org/v3/api provides access to associations between genes, diseases, and phenotypes using MONDO disease IDs, Human Phenotype Ontology (HPO) terms, and standard gene identifiers. No authentication is required; the service is free for academic use.

When to Use

• Mapping a disease (MONDO ID) to all associated causal genes and their evidence sources
• Retrieving phenotype profiles (HP terms) for a disease to build phenotypic similarity models
• Ranking candidate genes by phenotypic similarity to a patient's HPO symptom list
• Querying cross-species gene-phenotype associations (mouse, zebrafish, fly) for model organism comparisons
• Exploring rare disease gene-phenotype networks for diagnostic candidate generation
• Resolving entity metadata (gene symbol, disease name, phenotype label) from a MONDO/HP/HGNC ID
• Use opentargets-database instead when you need drug-target evidence scores or tractability data alongside disease associations
• Use clinvar-database when you need clinical pathogenicity classifications with submitter review status

Prerequisites

• Python packages: requests, pandas, matplotlib
• Data requirements: MONDO IDs (e.g., MONDO:0007374), HP term IDs (e.g., HP:0001250), or gene symbols/HGNC IDs
• Environment: internet connection; no API key required
• Rate limits: no published rate limit; use time.sleep(0.3) between batch requests; avoid bursts over 10 requests/second

bash
pip install requests pandas matplotlib

Quick Start

python
import requests

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def monarch_get(endpoint: str, params: dict = None) -> dict:
    """GET request to Monarch API; raises on HTTP errors."""
    r = requests.get(f"{MONARCH_API}{endpoint}", params=params, timeout=30)
    r.raise_for_status()
    return r.json()

# Get all genes associated with Marfan syndrome (MONDO:0007374)
result = monarch_get("/association/all", params={
    "subject": "MONDO:0007374",
    "category": "biolink:GeneToDiseaseAssociation",
    "limit": 10
})
print(f"Total gene associations: {result['total']}")
for item in result["items"][:5]:
    obj = item.get("object", {})
    print(f"  Gene: {obj.get('label', 'N/A')}  ({obj.get('id', 'N/A')})")
# Total gene associations: 3
# Gene: FBN1  (HGNC:3603)

Core API

Query 1: Disease-Gene Associations

Retrieve all genes associated with a disease by MONDO ID. Returns causal gene records with evidence metadata.

python
import requests
import pandas as pd
import time

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def monarch_get(endpoint, params=None):
    r = requests.get(f"{MONARCH_API}{endpoint}", params=params, timeout=30)
    r.raise_for_status()
    return r.json()

def get_disease_genes(mondo_id: str, limit: int = 200) -> pd.DataFrame:
    """Return DataFrame of genes associated with a disease."""
    result = monarch_get("/association/all", params={
        "subject": mondo_id,
        "category": "biolink:CausalGeneToDiseaseAssociation",
        "limit": limit
    })
    rows = []
    for item in result.get("items", []):
        obj = item.get("object", {})
        rows.append({
            "gene_id": obj.get("id"),
            "gene_symbol": obj.get("label"),
            "taxon": obj.get("taxon", {}).get("label") if obj.get("taxon") else None,
            "relation": item.get("predicate"),
            "evidence_count": len(item.get("evidence", [])),
        })
    return pd.DataFrame(rows)

# Cystic fibrosis (MONDO:0009861)
df = get_disease_genes("MONDO:0009861")
print(f"Genes for cystic fibrosis: {len(df)}")
print(df[["gene_symbol", "gene_id", "relation"]].to_string(index=False))
# Genes for cystic fibrosis: 1
# gene_symbol  gene_id    relation
#        CFTR  HGNC:1884  biolink:causes

Query 2: Disease-Phenotype Associations

Retrieve HPO phenotype terms linked to a disease. Useful for building phenotype profiles and similarity scoring.

python
def get_disease_phenotypes(mondo_id: str, limit: int = 200) -> pd.DataFrame:
    """Return DataFrame of phenotypes (HP terms) for a disease."""
    result = monarch_get("/association/all", params={
        "subject": mondo_id,
        "category": "biolink:DiseaseToPhenotypicFeatureAssociation",
        "limit": limit
    })
    rows = []
    for item in result.get("items", []):
        obj = item.get("object", {})
        rows.append({
            "hp_id": obj.get("id"),
            "phenotype": obj.get("label"),
            "frequency": item.get("frequency", {}).get("label") if item.get("frequency") else None,
            "onset": item.get("onset", {}).get("label") if item.get("onset") else None,
        })
    return pd.DataFrame(rows)

# Marfan syndrome (MONDO:0007374)
df = get_disease_phenotypes("MONDO:0007374", limit=50)
print(f"Phenotypes for Marfan syndrome: {len(df)}")
print(df[["phenotype", "hp_id", "frequency"]].head(8).to_string(index=False))
# Phenotypes for Marfan syndrome: 26
# phenotype                      hp_id        frequency
# Aortic root aneurysm        HP:0002616    HP:0040281  ...

Query 3: Entity Lookup

Retrieve metadata for any Monarch entity (gene, disease, phenotype) by its identifier.

python
def get_entity(entity_id: str) -> dict:
    """Retrieve metadata for a gene, disease, or phenotype by its ID."""
    result = monarch_get(f"/entity/{entity_id}")
    return result

# Look up HP:0001250 (Seizure)
hp = get_entity("HP:0001250")
print(f"Name: {hp.get('name')}")
print(f"ID: {hp.get('id')}")
print(f"Description: {hp.get('description', '')[:120]}")
print(f"Synonyms: {[s.get('val') for s in hp.get('synonyms', [])[:3]]}")
# Name: Seizure
# ID: HP:0001250
# Description: A seizure is an intermittent abnormality of nervous system physiology ...

# Look up a MONDO disease
disease = get_entity("MONDO:0007374")
print(f"\nDisease: {disease.get('name')}")
print(f"ID: {disease.get('id')}")

Query 4: Text Search for Entities

Search for entities by free-text label, useful for resolving disease names or phenotype terms to IDs.

python
def search_entities(query: str, category: str = None, limit: int = 10) -> list:
    """Search Monarch entities by label/synonym."""
    params = {"q": query, "limit": limit}
    if category:
        params["category"] = category
    result = monarch_get("/search", params=params)
    return result.get("items", [])

# Search for "Ehlers-Danlos" diseases
hits = search_entities("Ehlers-Danlos", category="biolink:Disease", limit=8)
for hit in hits:
    print(f"  {hit.get('id'):<25}  {hit.get('name', 'N/A')}")
# MONDO:0020066              Ehlers-Danlos syndrome
# MONDO:0007522              classical Ehlers-Danlos syndrome
# MONDO:0007528              hypermobile Ehlers-Danlos syndrome
# MONDO:0007523              kyphoscoliotic Ehlers-Danlos syndrome

Query 5: Gene-to-Disease Associations

Retrieve diseases associated with a gene. Useful for understanding a gene's disease spectrum.

python
def get_gene_diseases(gene_id: str, limit: int = 100) -> pd.DataFrame:
    """Return DataFrame of diseases associated with a gene."""
    result = monarch_get("/association/all", params={
        "subject": gene_id,
        "category": "biolink:GeneToDiseaseAssociation",
        "limit": limit
    })
    rows = []
    for item in result.get("items", []):
        obj = item.get("object", {})
        rows.append({
            "disease_id": obj.get("id"),
            "disease_name": obj.get("label"),
            "predicate": item.get("predicate"),
        })
    return pd.DataFrame(rows)

# Diseases caused by FBN1 (HGNC:3603)
df = get_gene_diseases("HGNC:3603")
print(f"Diseases linked to FBN1: {len(df)}")
print(df[["disease_name", "disease_id"]].head(5).to_string(index=False))
# Diseases linked to FBN1: 8
# disease_name                     disease_id
# Marfan syndrome                  MONDO:0007374
# Stiff skin syndrome              MONDO:0007926

Query 6: Gene-Phenotype Associations (Cross-Species)

Query phenotypes linked to a gene across species including mouse, zebrafish, and human.

python
def get_gene_phenotypes(gene_id: str, limit: int = 100) -> pd.DataFrame:
    """Return gene-phenotype associations, optionally across species."""
    result = monarch_get("/association/all", params={
        "subject": gene_id,
        "category": "biolink:GeneToPhenotypicFeatureAssociation",
        "limit": limit
    })
    rows = []
    for item in result.get("items", []):
        subj = item.get("subject", {})
        obj = item.get("object", {})
        rows.append({
            "gene_id": subj.get("id"),
            "gene_symbol": subj.get("label"),
            "taxon": subj.get("taxon", {}).get("label") if subj.get("taxon") else None,
            "phenotype_id": obj.get("id"),
            "phenotype": obj.get("label"),
        })
    return pd.DataFrame(rows)

# Phenotypes for human FBN1
df = get_gene_phenotypes("HGNC:3603")
print(f"FBN1 phenotype associations: {len(df)}")
print(df[["taxon", "phenotype"]].value_counts("taxon"))
# Homo sapiens    18
# Mus musculus     6

Query 7: Histopheno — Phenotype Distribution for a Disease

Retrieve summarized phenotype counts by anatomical system for a disease, useful for phenotype spectrum overviews.

python
def get_histopheno(mondo_id: str) -> dict:
    """Retrieve summarized phenotype distribution for a disease."""
    result = monarch_get(f"/histopheno/{mondo_id}")
    return result

hist = get_histopheno("MONDO:0007374")   # Marfan syndrome
items = hist.get("items", [])
print(f"Phenotype categories for Marfan syndrome ({len(items)} systems):")
for item in sorted(items, key=lambda x: x.get("count", 0), reverse=True)[:8]:
    print(f"  {item.get('label', 'N/A'):<40}  n={item.get('count', 0)}")
# Connective tissue                         n=12
# Cardiovascular system                     n=8
# Eye                                       n=6

Query 8: Phenotype-to-Gene Associations

Given a set of HP phenotype terms, retrieve associated genes — the basis of phenotype-matching tools.

python
def get_phenotype_genes(hp_id: str, limit: int = 50) -> pd.DataFrame:
    """Return genes associated with a phenotype term."""
    result = monarch_get("/association/all", params={
        "object": hp_id,
        "category": "biolink:GeneToPhenotypicFeatureAssociation",
        "limit": limit
    })
    rows = []
    for item in result.get("items", []):
        subj = item.get("subject", {})
        rows.append({
            "gene_id": subj.get("id"),
            "gene_symbol": subj.get("label"),
            "taxon": subj.get("taxon", {}).get("label") if subj.get("taxon") else None,
        })
    return pd.DataFrame(rows)

# HP:0001631 — Atrial septal defect
df = get_phenotype_genes("HP:0001631")
print(f"Genes associated with Atrial septal defect: {len(df)}")
print(df[df["taxon"] == "Homo sapiens"]["gene_symbol"].head(8).tolist())
# ['TBX5', 'GATA4', 'NKX2-5', 'MYH6', 'ACTC1', ...]

Key Concepts

Monarch Identifier System

Monarch uses ontology-based compact URIs (CURIEs) as identifiers:

| Prefix | Namespace | Example | |--------|-----------|---------| | MONDO | Mondo Disease Ontology | MONDO:0007374 (Marfan syndrome) | | HP | Human Phenotype Ontology | HP:0001250 (Seizure) | | HGNC | HGNC human genes | HGNC:3603 (FBN1) | | NCBIGene | NCBI Gene IDs | NCBIGene:2200 (FBN1) | | MGI | Mouse Genome Informatics | MGI:95489 (Fbn1 mouse) | | ZFIN | Zebrafish Information Network | ZFIN:ZDB-GENE-... |

Use the /search endpoint to convert free-text names to IDs before querying associations.

Association Categories

Monarch uses biolink model categories for associations:

| Category | Meaning | |----------|---------| | biolink:CausalGeneToDiseaseAssociation | Gene causes the disease | | biolink:DiseaseToPhenotypicFeatureAssociation | Disease → phenotype (HPO terms) | | biolink:GeneToPhenotypicFeatureAssociation | Gene → phenotype (any species) | | biolink:GeneToDiseaseAssociation | Any gene-disease link (broader) |

Use CausalGeneToDiseaseAssociation for pathogenic gene lists; use GeneToDiseaseAssociation for broader evidence including susceptibility loci.

Common Workflows

Workflow 1: Rare Disease Gene Prioritization

Goal: Given a set of HPO terms from a patient, retrieve all diseases with overlapping phenotypes and their causal genes.

python
import requests
import pandas as pd
import time

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def monarch_get(endpoint, params=None):
    r = requests.get(f"{MONARCH_API}{endpoint}", params=params, timeout=30)
    r.raise_for_status()
    return r.json()

# Patient HPO profile
patient_hp_terms = ["HP:0001250", "HP:0000252", "HP:0001263"]   # Seizure, Microcephaly, DD

gene_scores = {}
for hp_id in patient_hp_terms:
    result = monarch_get("/association/all", params={
        "object": hp_id,
        "category": "biolink:DiseaseToPhenotypicFeatureAssociation",
        "limit": 50
    })
    diseases = [item.get("subject", {}).get("id") for item in result.get("items", [])]
    # For each disease, get causal genes
    for disease_id in diseases[:5]:    # limit per phenotype for demo
        gene_result = monarch_get("/association/all", params={
            "subject": disease_id,
            "category": "biolink:CausalGeneToDiseaseAssociation",
            "limit": 20
        })
        for item in gene_result.get("items", []):
            gene_sym = item.get("object", {}).get("label", "")
            if gene_sym:
                gene_scores[gene_sym] = gene_scores.get(gene_sym, 0) + 1
        time.sleep(0.3)

# Rank genes by co-occurrence with patient phenotypes
df = pd.DataFrame(
    [(gene, score) for gene, score in gene_scores.items()],
    columns=["gene_symbol", "phenotype_overlap_score"]
).sort_values("phenotype_overlap_score", ascending=False)
print(f"Candidate genes ranked by phenotype overlap (n={len(df)})")
print(df.head(10).to_string(index=False))
df.to_csv("candidate_genes_phenotype_ranked.csv", index=False)

Workflow 2: Disease Phenotype Profile and Visualization

Goal: Retrieve all HPO terms for a disease, summarize by anatomical category, and plot a bar chart.

python
import requests
import pandas as pd
import matplotlib.pyplot as plt
import time

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def monarch_get(endpoint, params=None):
    r = requests.get(f"{MONARCH_API}{endpoint}", params=params, timeout=30)
    r.raise_for_status()
    return r.json()

mondo_id = "MONDO:0009861"   # Cystic fibrosis
disease_info = monarch_get(f"/entity/{mondo_id}")
disease_name = disease_info.get("name", mondo_id)

# Step 1: Get phenotype associations
result = monarch_get("/association/all", params={
    "subject": mondo_id,
    "category": "biolink:DiseaseToPhenotypicFeatureAssociation",
    "limit": 200
})
items = result.get("items", [])
print(f"Phenotypes for {disease_name}: {len(items)}")

# Step 2: Gather HP term labels
rows = []
for item in items:
    obj = item.get("object", {})
    rows.append({
        "hp_id": obj.get("id"),
        "phenotype": obj.get("label"),
        "frequency": item.get("frequency", {}).get("label") if item.get("frequency") else "Unknown"
    })
df = pd.DataFrame(rows)

# Step 3: Histopheno summary for bar chart
hist = monarch_get(f"/histopheno/{mondo_id}")
hist_items = sorted(hist.get("items", []), key=lambda x: x.get("count", 0), reverse=True)[:12]
systems = [x.get("label", "Other")[:25] for x in hist_items]
counts = [x.get("count", 0) for x in hist_items]

fig, ax = plt.subplots(figsize=(10, 5))
bars = ax.barh(systems[::-1], counts[::-1], color="#2196F3")
ax.bar_label(bars, fmt="%d", padding=3)
ax.set_xlabel("Phenotype Count")
ax.set_title(f"Phenotype Distribution by System\n{disease_name} ({mondo_id})")
plt.tight_layout()
plt.savefig("monarch_phenotype_distribution.png", dpi=150, bbox_inches="tight")
print(f"Saved monarch_phenotype_distribution.png ({len(df)} total phenotypes)")

# Step 4: Export HPO terms
df.to_csv(f"{mondo_id.replace(':', '_')}_phenotypes.csv", index=False)
print(df[["hp_id", "phenotype", "frequency"]].head(8).to_string(index=False))

Workflow 3: Cross-Species Gene-Disease Network

Goal: Build a table of disease-gene associations including mouse model genes for a list of rare diseases.

python
import requests
import pandas as pd
import time

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def monarch_get(endpoint, params=None):
    r = requests.get(f"{MONARCH_API}{endpoint}", params=params, timeout=30)
    r.raise_for_status()
    return r.json()

diseases = {
    "MONDO:0007374": "Marfan syndrome",
    "MONDO:0009861": "Cystic fibrosis",
    "MONDO:0007522": "Classical EDS",
}

all_rows = []
for mondo_id, disease_name in diseases.items():
    # Human causal genes
    result = monarch_get("/association/all", params={
        "subject": mondo_id,
        "category": "biolink:CausalGeneToDiseaseAssociation",
        "limit": 50
    })
    for item in result.get("items", []):
        obj = item.get("object", {})
        all_rows.append({
            "disease_id": mondo_id,
            "disease_name": disease_name,
            "gene_id": obj.get("id"),
            "gene_symbol": obj.get("label"),
            "species": "Homo sapiens",
        })
    time.sleep(0.3)

df = pd.DataFrame(all_rows)
df.to_csv("rare_disease_gene_network.csv", index=False)
print(f"Associations collected: {len(df)}")
print(df.groupby("disease_name")["gene_symbol"].apply(list).to_string())

Key Parameters

| Parameter | Function/Endpoint | Default | Range / Options | Effect | |-----------|-------------------|---------|-----------------|--------| | category | /association/all | (none) | biolink:CausalGeneToDiseaseAssociation, biolink:DiseaseToPhenotypicFeatureAssociation, biolink:GeneToPhenotypicFeatureAssociation, biolink:GeneToDiseaseAssociation | Filters association type | | subject | /association/all | (none) | CURIE string (e.g., MONDO:0007374) | Source entity (disease or gene) | | object | /association/all | (none) | CURIE string (e.g., HP:0001250) | Target entity (phenotype or disease) | | limit | /association/all, /search | 20 | 1–500 | Max items returned per page | | offset | /association/all | 0 | integer | Pagination offset | | q | /search | (none) | free-text string | Label/synonym text search | | entity_id | /entity/{id} | (none) | CURIE string | Entity ID for metadata lookup | | mondo_id | /histopheno/{id} | (none) | MONDO CURIE | Disease ID for phenotype histogram |

Best Practices

1. Resolve names to IDs first using /search: All association queries require CURIE IDs (e.g., MONDO:0007374), not free-text. Use search_entities() to resolve "Marfan syndrome" → MONDO:0007374 before querying associations.

1. Use CausalGeneToDiseaseAssociation for gene lists, not GeneToDiseaseAssociation: The broader category includes susceptibility associations and ambiguous links. Causal associations have stronger evidence support.

1. Paginate large result sets with offset: The default limit is 20 and max is 500. Check result["total"] and paginate with offset increments to retrieve all records for diseases with many phenotypes:

python total = monarch_get("/association/all", params={"subject": mondo_id, "category": "...", "limit": 1})["total"] all_items = [] for offset in range(0, total, 200): batch = monarch_get("/association/all", params={"subject": mondo_id, "category": "...", "limit": 200, "offset": offset}) all_items.extend(batch.get("items", [])) time.sleep(0.3)

1. Use time.sleep(0.3) between requests in batch loops: The API is publicly accessible without rate limit documentation; polite access avoids throttling for multi-disease workflows.

1. Cross-reference gene IDs with HGNC for human genes: Monarch may return HGNC:XXXX or NCBIGene:XXXX IDs. Use the HGNC prefix for downstream tools that require HGNC; use the /entity/{id} endpoint to retrieve the alternative ID.

Common Recipes

Recipe: Resolve Disease Name to MONDO ID

When to use: Convert a disease name string to the canonical MONDO identifier before querying.

python
import requests

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def resolve_disease(name: str, top_n: int = 5) -> list:
    """Search for disease name and return top MONDO ID candidates."""
    r = requests.get(f"{MONARCH_API}/search",
                     params={"q": name, "category": "biolink:Disease", "limit": top_n},
                     timeout=15)
    r.raise_for_status()
    return [(h.get("id"), h.get("name")) for h in r.json().get("items", [])]

candidates = resolve_disease("Huntington disease")
for mondo_id, label in candidates:
    print(f"  {mondo_id:<25}  {label}")
# MONDO:0007739              Huntington disease
# MONDO:0024321              Huntington disease-like 1

Recipe: Batch Disease-Gene Lookup

When to use: Retrieve causal genes for a list of MONDO IDs in one call each, with results combined into a single DataFrame.

python
import requests
import pandas as pd
import time

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def get_causal_genes(mondo_id):
    r = requests.get(f"{MONARCH_API}/association/all",
                     params={"subject": mondo_id,
                             "category": "biolink:CausalGeneToDiseaseAssociation",
                             "limit": 100},
                     timeout=30)
    r.raise_for_status()
    data = r.json()
    return [(item.get("object", {}).get("id"), item.get("object", {}).get("label"))
            for item in data.get("items", [])]

disease_ids = ["MONDO:0007374", "MONDO:0009861", "MONDO:0007739"]
rows = []
for mondo_id in disease_ids:
    for gene_id, gene_sym in get_causal_genes(mondo_id):
        rows.append({"disease_id": mondo_id, "gene_id": gene_id, "gene_symbol": gene_sym})
    time.sleep(0.3)

df = pd.DataFrame(rows)
print(df.to_string(index=False))
df.to_csv("batch_disease_genes.csv", index=False)
print(f"\nTotal disease-gene pairs: {len(df)}")

Recipe: HPO Profile Similarity Seed

When to use: Retrieve disease HPO profiles to use as input seeds for phenotype similarity tools (e.g., Phenomizer, LIRICAL).

python
import requests, json

MONARCH_API = "https://api.monarchinitiative.org/v3/api"

def get_hp_profile(mondo_id, limit=500):
    """Return list of HP term IDs for a disease."""
    r = requests.get(f"{MONARCH_API}/association/all",
                     params={"subject": mondo_id,
                             "category": "biolink:DiseaseToPhenotypicFeatureAssociation",
                             "limit": limit},
                     timeout=30)
    r.raise_for_status()
    items = r.json().get("items", [])
    return [item.get("object", {}).get("id") for item in items if item.get("object", {}).get("id")]

hp_terms = get_hp_profile("MONDO:0007374")   # Marfan syndrome
print(f"HP terms for Marfan syndrome: {len(hp_terms)}")
print(hp_terms[:8])
# ['HP:0002616', 'HP:0001166', 'HP:0000768', 'HP:0001083', ...]

# Save for downstream phenotype similarity tool input
with open("MONDO_0007374_hp_profile.json", "w") as f:
    json.dump({"disease": "MONDO:0007374", "hpo_terms": hp_terms}, f, indent=2)
print("Saved MONDO_0007374_hp_profile.json")

Troubleshooting

| Problem | Cause | Solution | |---------|-------|----------| | Empty items list | Wrong category string or entity has no associations of that type | Check the category name exactly; try biolink:GeneToDiseaseAssociation as a broader fallback | | 404 Not Found for /entity/{id} | Malformed CURIE or deprecated ID | Verify ID format (e.g., MONDO:0007374 not MONDO_0007374); use /search to find current IDs | | total is 0 but entity exists | Subject/object direction reversed | Check whether you need subject or object parameter; gene→disease uses subject=gene_id; disease→phenotype uses subject=disease_id | | requests.exceptions.Timeout | API overloaded or network issue | Increase timeout=60; retry with exponential backoff | | Gene ID returned as NCBIGene instead of HGNC | Monarch may use either namespace | Use /entity/{id} to retrieve xrefs field for alternative IDs including HGNC, Ensembl | | Results differ between API calls for same entity | Monarch knowledge graph is updated regularly | Pin your data collection date; note API version in methods section | | Rate-limited or slow responses | Too many rapid requests | Add time.sleep(0.5) between batch requests; use limit=200 to reduce total requests |

Related Skills

• clinvar-database — clinical pathogenicity classifications for specific variants (complements Monarch's gene-disease associations)
• gwas-database — GWAS Catalog associations for common variants and traits
• opentargets-database — drug-target evidence with tractability and safety scores
• ensembl-database — gene/transcript annotation and cross-species orthology via Ensembl REST API
• gseapy-gene-enrichment — gene set enrichment analysis using the Monarch-derived gene lists

References

• Monarch Initiative API v3 — Interactive Swagger/OpenAPI documentation
• Monarch Initiative — Main portal with disease-gene-phenotype knowledge graph browser
• Mungall et al., Genome Biology 2017 — Monarch Integration methodology paper
• Mondo Disease Ontology — MONDO ID reference and ontology browser
• Human Phenotype Ontology — HPO term browser and clinical applications