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

6,201–6,300 of 23,730, alphabetically

corpus callosum dysgenesis cleft spasmMondoMONDO:0022873
corpus callosum dysgenesis hypopituitarismMondoMONDO:0022874
corpus callosum dysgenesis X-linked recessiveMondoMONDO:0022872
corpus callosum lipomaMondoMONDO:0003845
corpus callosum oligodendrogliomaMondoMONDO:0000519

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

corpus callosum, agenesis of

MondoMONDO:0009022

corpus luteum cystMondoMONDO:0001625

corpus uteri neoplasmMondoMONDO:0021254

cortada Koussef Matsumoto syndromeMondoMONDO:0022875

Cortes Lacassie syndromeMondoMONDO:0022876

cortical blindnessMondoMONDO:0001385

cortical blindness-intellectual disability-polydactyly syndromeMondoMONDO:0009024

cortical cataractMondoMONDO:0045051

cortical deafnessMondoMONDO:0000670

cortical dysplasia-focal epilepsy syndromeMondoMONDO:0012400

cortical dysplasia, complex, with other brain malformations 10MondoMONDO:0032866

cortical dysplasia, complex, with other brain malformations 11MondoMONDO:0859332

cortical dysplasia, complex, with other brain malformations 12MondoMONDO:0957217

cortical dysplasia, complex, with other brain malformations 9MondoMONDO:0032578

cortical senile cataractMondoMONDO:0001749

cortical thymomaMondoMONDO:0003915

corticobasal degeneration disorderMondoMONDO:0022308

corticobasal syndromeMondoMONDO:0018696

corticosteroid myopathyMondoMONDO:0100636

corticosteroid-binding globulin deficiencyMondoMONDO:0012675

corticosteroid-induced osteoporosisMondoMONDO:0024651

corticosteroid-sensitive aseptic abscess syndromeMondoMONDO:0018900

corticosterone methyloxidase type 1 deficiencyMondoMONDO:0008751

corticosterone methyloxidase type 2 deficiencyMondoMONDO:0012524

cortisol-producing adrenal cortex adenomaMondoMONDO:0006174

cortisone reductase deficiencyMondoMONDO:0000193

cortisone reductase deficiency 1MondoMONDO:0011503

cortisone reductase deficiency 2MondoMONDO:0013842

Costello syndromeMondoMONDO:0009026

cote katsantoni syndromeMondoMONDO:0022311

cough variant asthmaMondoMONDO:0001491

coumarin resistanceMondoMONDO:0007390

COVID-19MondoMONDO:0100096

COVID-19–associated multisystem inflammatory syndrome in adultsMondoMONDO:0100319

COVID-19–associated multisystem inflammatory syndrome in childrenMondoMONDO:0100163

Cowden diseaseMondoMONDO:0016063

Cowden syndrome 1MondoMONDO:0008021

Cowden syndrome 2MondoMONDO:0012878

Cowden syndrome 3MondoMONDO:0014045

Cowden syndrome 4MondoMONDO:0014046

Cowden syndrome 5MondoMONDO:0014047

Cowden syndrome 6MondoMONDO:0014048

Cowden syndrome 7MondoMONDO:0014802

cowpoxMondoMONDO:0005720

COX deficiency, benign infantile mitochondrial myopathyMondoMONDO:0957524

coxa varaMondoMONDO:0007391

coxoauricular syndromeMondoMONDO:0007392

coxopodopatellar syndromeMondoMONDO:0007841

coxsackievirus infectious diseaseMondoMONDO:0005721

CPOX-related hereditary coproporphyriaMondoMONDO:0800180

Cramp-fasciculation syndromeMondoMONDO:0035586

Crandall syndromeMondoMONDO:0016067

Crane-Heise syndromeMondoMONDO:0009028

cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delayMondoMONDO:0957563

cranial nerve neoplasmMondoMONDO:0002633

cranial nerve neuropathyMondoMONDO:0003569

cranial nerve palsyMondoMONDO:0002782

cranial nerves, congenital paresis ofMondoMONDO:0009029

cranial nerves, recurrent paresis ofMondoMONDO:0009030

cranial neuralgiaMondoMONDO:0016374

cranial nodular fasciitisMondoMONDO:0004186

cranio-osteoarthropathyMondoMONDO:0015466

cranioacrofacial syndromeMondoMONDO:0007393

craniodiaphyseal dysplasiaMondoMONDO:0009031

craniodiaphyseal dysplasia, autosomal dominantMondoMONDO:0021021

craniodigital syndrome-intellectual disability syndromeMondoMONDO:0015463

cranioectodermal dysplasiaMondoMONDO:0009032

cranioectodermal dysplasia 1MondoMONDO:0021093

cranioectodermal dysplasia 2MondoMONDO:0013323

cranioectodermal dysplasia 3MondoMONDO:0013573

cranioectodermal dysplasia 4MondoMONDO:0013719

cranioectodermal dysplasia 5MondoMONDO:0976269

cranioectodermal dysplasia 6MondoMONDO:0979883

craniofacial and skeletal defectsMondoMONDO:0022883

craniofacial anomalies and anterior segment dysgenesis syndromeMondoMONDO:0013618

craniofacial conodysplasiaMondoMONDO:0019406

craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1MondoMONDO:0800436

craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndromeMondoMONDO:0031329

craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2MondoMONDO:0859567

craniofacial dysostosis arthrogryposis progeroid appearanceMondoMONDO:0022884

craniofacial dysplasia - osteopenia syndromeMondoMONDO:0012634

craniofacial dyssynostosisMondoMONDO:0009034

craniofacial dystoniaMondoMONDO:0000486

craniofacial microsomiaMondoMONDO:0015397

craniofacial microsomia 1MondoMONDO:0958175

craniofacial microsomia 2MondoMONDO:0958194

craniofacial-deafness-hand syndromeMondoMONDO:0007395

craniofaciocardiohepatic syndromeMondoMONDO:0978295

craniofaciofrontodigital syndromeMondoMONDO:0007259

craniofrontonasal dysplasia-Poland anomaly syndromeMondoMONDO:0015464

craniofrontonasal syndromeMondoMONDO:0010570

craniofrontonasal syndrome Teebi typeMondoMONDO:0022887

craniolenticulosutural dysplasiaMondoMONDO:0011911

craniometadiaphyseal dysplasia, wormian bone typeMondoMONDO:0010014

craniometadiaphyseal osteosclerosis with hip dysplasiaMondoMONDO:0957832

Page 63 of 238

Next First Last