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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

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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

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Catalyst

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

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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

20,301–20,400 of 23,730, alphabetically

secondary hyperparathyroidismMondoMONDO:0006964
secondary hyperparathyroidism of renal originMondoMONDO:0001530
secondary hypertensionMondoMONDO:0001200
secondary hyperthyroidismMondoMONDO:1060201
secondary hypertrophic osteoarthropathyMondoMONDO:0006965

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

secondary hypoparathyroidism due to impaired parathormon secretion

MondoMONDO:0015357

secondary intestinal lymphangiectasiaMondoMONDO:0019574

secondary lacrimal atrophyMondoMONDO:0002124

secondary malignant neoplasmMondoMONDO:0024881

secondary mast cell activation syndromeMondoMONDO:0100006

secondary neonatal autoimmune diseaseMondoMONDO:0018356

secondary neoplasmMondoMONDO:0024882

secondary non-traumatic avascular necrosisMondoMONDO:0018376

secondary Parkinson diseaseMondoMONDO:0006966

secondary polyarteritis nodosaMondoMONDO:0018594

secondary polycythemiaMondoMONDO:0020115

secondary progressive multiple sclerosisMondoMONDO:0000450

secondary pulmonary alveolar proteinosisMondoMONDO:0018483

secondary pulmonary hemosiderosisMondoMONDO:0020553

secondary sclerosing cholangitisMondoMONDO:0018647

secondary short bowel syndromeMondoMONDO:0019802

secondary syphilisMondoMONDO:0002897

secondary syringomyeliaMondoMONDO:0020509

secondary trimethylaminuriaMondoMONDO:0100041

secondary vasculitisMondoMONDO:0018640

secondary vitreoretinal degenerationMondoMONDO:0001457

secretory component deficiencyMondoMONDO:0010019

secretory diarrheaMondoMONDO:0000249

secretory diarrhea, myopathy, and deafnessMondoMONDO:0011854

secretory meningiomaMondoMONDO:0003055

secretory uterine corpus endometrioid adenocarcinomaMondoMONDO:0004174

segmental arterial mediolysisMondoMONDO:0957452

segmental dystoniaMondoMONDO:0000479

segmental odontomaxillary dysplasiaMondoMONDO:0019029

segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeMondoMONDO:0015293

segmental progressive overgrowth syndrome with fibroadipose hyperplasiaMondoMONDO:0017812

segmental spinal dysgenesisMondoMONDO:0958275

seizures-intellectual disability due to hydroxylysinuria syndromeMondoMONDO:0009373

seizures-scoliosis-macrocephaly syndromeMondoMONDO:0014731

seizures, benign familial infantile, 2MondoMONDO:0011593

seizures, benign familial infantile, 3MondoMONDO:0011904

seizures, benign familial infantile, 4MondoMONDO:0012965

seizures, benign familial infantile, 5MondoMONDO:0014903

seizures, benign familial neonatal, 1MondoMONDO:0007365

seizures, benign familial neonatal, 2MondoMONDO:0007366

seizures, benign familial neonatal, 3MondoMONDO:0011990

seizures, benign familial neonatal, autosomal recessiveMondoMONDO:0010021

seizures, early-onset, with neurodegeneration and brain calcificationsMondoMONDO:0030033

selective IgA deficiency diseaseMondoMONDO:0001341

selective IgD deficiency diseaseMondoMONDO:0004165

selective IgE deficiency diseaseMondoMONDO:0003738

selective IgG immunodeficiencyMondoMONDO:0045045

selective IgG subclass deficiencyMondoMONDO:0001901

selective IgM deficiencyMondoMONDO:0018039

selective immunoglobulin deficiency diseaseMondoMONDO:0003739

selective intrauterine growth restrictionMondoMONDO:0850015

selective peripheral resistance to thyroid hormoneMondoMONDO:0020711

selective pituitary resistance to thyroid hormoneMondoMONDO:0007784

self-healing collodion babyMondoMONDO:0017267

self-healing papular mucinosisMondoMONDO:0019582

self-limited childhood occipital epilepsyMondoMONDO:0007558

self-limited epilepsy with autonomic seizuresMondoMONDO:0020307

self-limited epilepsy with centrotemporal spikesMondoMONDO:0007295

self-limited familial infantile epilepsyMondoMONDO:0100024

self-limited familial neonatal epilepsyMondoMONDO:0100023

self-limited familial neonatal-infantile epilepsyMondoMONDO:0100208

self-limited neonatal seizuresMondoMONDO:0800479

sella turcica neoplasmMondoMONDO:0002720

sella turcica, bridgedMondoMONDO:0008424

semantic agnosiaMondoMONDO:0000677

semantic dementiaMondoMONDO:0010857

semicircular canal dehiscence syndromeMondoMONDO:0018484

semilobar holoprosencephalyMondoMONDO:0700419

seminal vesicle acute gonorrheaMondoMONDO:0000222

seminal vesicle adenocarcinomaMondoMONDO:0001993

seminal vesicle chronic gonorrheaMondoMONDO:0001025

seminal vesicle cystadenomaMondoMONDO:0003609

seminal vesicle tumorMondoMONDO:0002790

seminomaMondoMONDO:0003001

Sener syndromeMondoMONDO:0011637

Sengers syndromeMondoMONDO:0008922

senile atrophy of choroidMondoMONDO:0004879

senile cataractMondoMONDO:0004847

senile degeneration of brainMondoMONDO:0001987

senile ectropionMondoMONDO:0001695

senile entropionMondoMONDO:0001591

senile plaque formationMondoMONDO:0010022

senile reticular retinal degenerationMondoMONDO:0001453

Senior-Boichis syndromeMondoMONDO:0019394

Senior-Loken syndromeMondoMONDO:0017842

Senior-Loken syndrome 1MondoMONDO:0009962

senior-loken syndrome 3MondoMONDO:0011755

Senior-Loken syndrome 4MondoMONDO:0011756

Senior-Loken syndrome 5MondoMONDO:0012225

Senior-Loken syndrome 6MondoMONDO:0012433

Senior-Loken syndrome 7MondoMONDO:0013326

Senior-Loken syndrome 8MondoMONDO:0014579

Senior-Loken syndrome 9MondoMONDO:0014712

sennetsu feverMondoMONDO:0000332

sensorineural hearing loss disorderMondoMONDO:0020678

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