Skip to content

Reference

Evidence

CompoundsSubstances with curated findings
OutcomesMeasured endpoints
ProteinsTransporters and enzymes
InteractionsPairs that share biology
PapersEvery paper a finding cites
ArticlesReadings of the evidence

Chemistry

ReactionsRhea and Human-GEM, by subsystem
ReachWhat a compound can become

Reference layer

PathwaysReactions grouped under one name
ProcessesWhat proteins are annotated as doing
AnatomyTissues, by what is expressed there
Cell typesCells, by what is expressed there
OrganismsSpecies a compound is prepared from
MaterialsSubstances that are not one molecule
AssessmentsRegulatory determinations, transcribed
DiseasesFeatures, genes, and where each sits

Atlas Graph Twin Access

Search the graph

Reference

Evidence

Compounds
Outcomes
Proteins
Interactions
Papers
Articles

Chemistry

Reactions
Reach

Reference layer

Pathways
Processes
Anatomy
Cell types
Organisms
Materials
Assessments
Diseases

Atlas Graph Twin Access

Loading the page.

Catalyst

Computational infrastructure for human biology, built on a provenance-aware knowledge graph. Findings retain their sources; research and simulation are the next layers.

The graph

Compounds
Outcomes
Proteins
Atlas
Interactions
Papers
Articles
Graph
Search

Reference layer

Pathways
Processes
Anatomy
Cell types
Organisms
Materials
Assessments
Diseases
Reactions
Reach

How it works

Mission
Method
Twin
How to read the evidence
Sources and licences

Build on it

Access
In your assistant
For agents
Query the graph
Bulk export

A reference for what the literature reports. Not medical advice.

© 2026 CatalystPrivacy TermsReference data under the licences listed on the attribution page.

Index

Diseases

Names from Mondo, HPO and GenCC

diseases in the graph: 23,730

Filter diseases by name

#a b c d e f g h i j k l m n o p q r s t u v w x y z

2,267 of 23,730 begin with P

peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domainMondoMONDO:0100265
peroxisome biogenesis disorder due to PEX6 defectMondoMONDO:0100263
peroxisome biogenesis disorder due to PEX7 defectMondoMONDO:0100272
peroxisome biogenesis disorder type 3BMondoMONDO:0009959
peroxisome biogenesis disorder, complementation group 2MondoMONDO:0800298

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

peroxisome biogenesis disorder, complementation group 3

MondoMONDO:0800364

peroxisome biogenesis disorder, complementation group KMondoMONDO:0800365

Perrault syndromeMondoMONDO:0017312

Perrault syndrome 1MondoMONDO:0009300

Perrault syndrome 2MondoMONDO:0013972

Perrault syndrome 3MondoMONDO:0013588

Perrault syndrome 4MondoMONDO:0014126

Perrault syndrome 5MondoMONDO:0014504

Perrault syndrome 6MondoMONDO:0033047

Perrault syndrome 7MondoMONDO:0976232

Perry syndromeMondoMONDO:0008201

persian gulf syndromeMondoMONDO:0005907

persistent atrial fibrillationMondoMONDO:1030009

persistent eustachian valveMondoMONDO:0020449

persistent fetal circulation syndromeMondoMONDO:0022430

persistent fifth aortic archMondoMONDO:0020414

persistent hyperplastic primary vitreousMondoMONDO:0019631

persistent hyperplastic primary vitreous, autosomal dominantMondoMONDO:0012653

persistent hyperplastic primary vitreous, autosomal recessiveMondoMONDO:0009097

persistent idiopathic facial painMondoMONDO:0018362

persistent left superior vena cava connecting to the left-sided atriumMondoMONDO:0020440

persistent Mullerian duct syndromeMondoMONDO:0009857

persistent placoid maculopathyMondoMONDO:0019973

persistent polyclonal B-cell lymphocytosisMondoMONDO:0011672

persistent tachypnoe of infancyMondoMONDO:0800109

persistent tachypnoe of infancy, aberrantMondoMONDO:0800110

persistent tachypnoe of infancy, usualMondoMONDO:0800111

persistent truncus arteriosusMondoMONDO:0018072

personality disorderMondoMONDO:0002028

pertussisMondoMONDO:0005077

pervasive developmental disorderMondoMONDO:0000594

pes anserinus tendinitis or bursitisMondoMONDO:0001533

pestivirus infectious diseaseMondoMONDO:0005909

Peters anomalyMondoMONDO:0011414

Peters anomaly-cataract syndromeMondoMONDO:0015095

Peters plus syndromeMondoMONDO:0009856

petroclival meningiomaMondoMONDO:0004367

petrositisMondoMONDO:0001109

petrous apex meningiomaMondoMONDO:0004238

Peutz-Jeghers polypMondoMONDO:0006365

Peutz-Jeghers polyp of the stomachMondoMONDO:0006366

Peutz-Jeghers syndromeMondoMONDO:0008280

Peyronie diseaseMondoMONDO:0008231

PFAPA syndromeMondoMONDO:0018540

pfeiffer rockelein syndromeMondoMONDO:0043172

Pfeiffer syndromeMondoMONDO:0007043

Pfeiffer syndrome type 1MondoMONDO:0019659

Pfeiffer syndrome type 2MondoMONDO:0019660

Pfeiffer syndrome type 3MondoMONDO:0019661

Pfeiffer Tietze Welte syndromeMondoMONDO:0043174

Pfeiffer-Palm-Teller syndromeMondoMONDO:0009858

PGM1-congenital disorder of glycosylationMondoMONDO:0013968

PHACE syndromeMondoMONDO:0011676

phacoanaphylactic uveitisMondoMONDO:0016207

phacogenic glaucomaMondoMONDO:0001554

phacolytic glaucomaMondoMONDO:0001553

phaeohyphomycosisMondoMONDO:0001867

phagocyte bactericidal dysfunctionMondoMONDO:0005910

phagocytic cell dysfunctionMondoMONDO:0024627

phagocytosis, plasma-related defect 1NMondoMONDO:0008232

phakomatosis cesioflammeaMondoMONDO:0019325

phakomatosis cesiomarmorataMondoMONDO:0019326

phakomatosis pigmentokeratoticaMondoMONDO:0017317

phakomatosis pigmentovascularisMondoMONDO:0017318

phakomatosis spiloroseaMondoMONDO:0019327

phalangeal microgeodic syndromeMondoMONDO:0018128

phalanx chondromaMondoMONDO:0000516

PHARC syndromeMondoMONDO:0012984

pharyngeal adenoid cystic carcinomaMondoMONDO:0006367

pharyngeal squamous cell carcinomaMondoMONDO:0000536

pharyngeal-cervical-brachial variant of Guillain-Barre syndromeMondoMONDO:0016496

pharyngitisMondoMONDO:0002258

pharyngoconjunctival feverMondoMONDO:0005911

pharynx cancerMondoMONDO:0005517

pharynx carcinoma in situMondoMONDO:0000372

pharynx neoplasmMondoMONDO:0021246

PHAVER syndromeMondoMONDO:0009859

Phelan-McDermid syndromeMondoMONDO:0011652

Phelan-McDermid syndrome due to 22q13.3 deletionMondoMONDO:0971068

Phelan-McDermid syndrome due to SHANK3 mutationMondoMONDO:0971069

phencyclidine abuseMondoMONDO:0005912

phenformin 4-hydroxylationMondoMONDO:0009860

phenobarbital embryopathyMondoMONDO:0016015

phenylketonuriaMondoMONDO:0009861

phenytoin or carbamazepine toxicityMondoMONDO:0033181

phenytoin toxicityMondoMONDO:0060690

pheochromocytomaMondoMONDO:0008233

pheochromocytoma-islet cell tumor syndromeMondoMONDO:0008235

pheochromocytoma-paragangliomaMondoMONDO:0035540

pheochromocytoma/paraganglioma syndrome 1MondoMONDO:0008192

pheochromocytoma/paraganglioma syndrome 2MondoMONDO:0011121

pheochromocytoma/paraganglioma syndrome 3MondoMONDO:0011544

pheochromocytoma/paraganglioma syndrome 4MondoMONDO:0007273

pheochromocytoma/paraganglioma syndrome 5MondoMONDO:0013602

pheochromocytoma/paraganglioma syndrome 6MondoMONDO:0032767

Page 9 of 23

Next First Last