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Evidence

CompoundsSubstances with curated findings
OutcomesMeasured endpoints
ProteinsTransporters and enzymes
InteractionsPairs that share biology
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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

13,001–13,100 of 23,730, alphabetically

leptomeningeal sarcomaMondoMONDO:0004330
leptomyelolipomaMondoMONDO:0017084
leptospirosisMondoMONDO:0005825
Leri pleonosteosisMondoMONDO:0007894
Leri-Weill dyschondrosteosisMondoMONDO:0007481
Leriche syndromeMondo

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

MONDO:0043683

Lesch-Nyhan phenotype with normal HGPRTMondoMONDO:0010642

Lesch-Nyhan syndromeMondoMONDO:0010298

lesion of sciatic nerveMondoMONDO:0001543

Lessel-Kreienkamp syndromeMondoMONDO:0030897

lessel-kubisch syndromeMondoMONDO:0032868

lethal acantholytic epidermolysis bullosaMondoMONDO:0012323

lethal arteriopathy syndrome due to fibulin-4 deficiencyMondoMONDO:0017818

lethal arthrogryposis-anterior horn cell disease syndromeMondoMONDO:0012750

lethal chondrodysplasia, Seller typeMondoMONDO:0011064

lethal congenital contracture syndromeMondoMONDO:0017436

lethal congenital contracture syndrome 1MondoMONDO:0009670

lethal congenital contracture syndrome 11MondoMONDO:0014965

lethal congenital contracture syndrome 12MondoMONDO:0981031

lethal congenital contracture syndrome 2MondoMONDO:0011868

lethal congenital contracture syndrome 3MondoMONDO:0012656

lethal congenital contracture syndrome 4MondoMONDO:0013965

lethal congenital contracture syndrome 6MondoMONDO:0014549

lethal congenital contracture syndrome 7MondoMONDO:0014569

lethal congenital contracture syndrome 8MondoMONDO:0014570

lethal congenital contracture syndrome 9MondoMONDO:0014670

lethal congenital glycogen storage disease of heartMondoMONDO:0009867

lethal faciocardiomelic dysplasiaMondoMONDO:0009204

lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndromeMondoMONDO:0014552

lethal hemolytic anemia-genital anomalies syndromeMondoMONDO:0010891

lethal hydranencephaly-diaphragmatic hernia syndromeMondoMONDO:0018810

lethal infantile mitochondrial myopathyMondoMONDO:0010792

lethal Kniest-like dysplasiaMondoMONDO:0009498

lethal Larsen-like syndromeMondoMONDO:0009512

lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndromeMondoMONDO:0014976

lethal multiple pterygium syndromeMondoMONDO:0009668

lethal occipital encephalocele-skeletal dysplasia syndromeMondoMONDO:0013740

lethal omphalocele-cleft palate syndromeMondoMONDO:0009780

lethal osteosclerotic bone dysplasiaMondoMONDO:0009821

lethal polymalformative syndrome, Boissel typeMondoMONDO:0013050

lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutationMondoMONDO:0036217

lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene clusterMondoMONDO:0036218

lethal recessive chondrodysplasiaMondoMONDO:0015425

lethal short-limb skeletal dysplasia, Al Gazali typeMondoMONDO:0011051

letrozole toxicityMondoMONDO:0035350

letterer-Siwe diseaseMondoMONDO:0009519

leukemiaMondoMONDO:0005059

leukemia, acute lymphoblastic, susceptibility to, 3MondoMONDO:0014241

leukemia, acute lymphocytic, susceptibility to, 1MondoMONDO:0013108

leukemia, acute lymphocytic, susceptibility to, 2MondoMONDO:0013109

leukemia, acute myelocytic, with polyposis coli and colon cancerMondoMONDO:0009521

leukemia, acute myeloid, susceptibility toMondoMONDO:0100173

leukemia, acute, X-linkedMondoMONDO:0700060

leukemia, chronic lymphocytic, susceptibility to, 1MondoMONDO:0012318

leukemia, chronic lymphocytic, susceptibility to, 2MondoMONDO:0007190

leukemia, chronic lymphocytic, susceptibility to, 3MondoMONDO:0012934

leukemia, chronic lymphocytic, susceptibility to, 4MondoMONDO:0012935

leukemia, chronic lymphocytic, susceptibility to, 5MondoMONDO:0012936

leukemia, myeloid, accelerated-phaseMondoMONDO:0021367

leukemoid reactionMondoMONDO:0006829

leukocyte adhesion deficiencyMondoMONDO:0017570

leukocyte adhesion deficiency 1MondoMONDO:0007293

leukocyte adhesion deficiency 3MondoMONDO:0013016

leukocyte adhesion deficiency type IIMondoMONDO:0009953

leukocyte disorderMondoMONDO:0004805

leukocyte nuclear appendages, hereditary prevalence ofMondoMONDO:0007898

leukodystrophyMondoMONDO:0019046

leukodystrophy and acquired microcephaly with or without dystonia;MondoMONDO:0014766

leukodystrophy, adult-onset, autosomal dominant, without amyloid angiopathyMondoMONDO:0979226

leukodystrophy, childhood-onset, remittingMondoMONDO:0859246

leukodystrophy, demyelinating, adult-onsetMondoMONDO:0976138

leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypicalMondoMONDO:0700286

leukodystrophy, demyelinating, adult-onset, autosomal dominant, typicalMondoMONDO:0700295

leukodystrophy, hypomyelinating, 10MondoMONDO:0014632

leukodystrophy, hypomyelinating, 11MondoMONDO:0014666

leukodystrophy, hypomyelinating, 12MondoMONDO:0014732

leukodystrophy, hypomyelinating, 13MondoMONDO:0014813

leukodystrophy, hypomyelinating, 14MondoMONDO:0033486

leukodystrophy, hypomyelinating, 15MondoMONDO:0054782

leukodystrophy, hypomyelinating, 16MondoMONDO:0054791

leukodystrophy, hypomyelinating, 17MondoMONDO:0054817

leukodystrophy, hypomyelinating, 18MondoMONDO:0032730

leukodystrophy, hypomyelinating, 19, transient infantileMondoMONDO:0032871

leukodystrophy, hypomyelinating, 2MondoMONDO:0012125

leukodystrophy, hypomyelinating, 20MondoMONDO:0033657

leukodystrophy, hypomyelinating, 21MondoMONDO:0030263

leukodystrophy, hypomyelinating, 22MondoMONDO:0025701

leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathyMondoMONDO:0030514

leukodystrophy, hypomyelinating, 24MondoMONDO:0859242

leukodystrophy, hypomyelinating, 25MondoMONDO:0859378

leukodystrophy, hypomyelinating, 26, with chondrodysplasiaMondoMONDO:0859518

leukodystrophy, hypomyelinating, 27MondoMONDO:0958018

leukodystrophy, hypomyelinating, 28MondoMONDO:0975833

leukodystrophy, hypomyelinating, 3MondoMONDO:0009843

leukodystrophy, hypomyelinating, 4MondoMONDO:0012824

leukodystrophy, hypomyelinating, 5MondoMONDO:0012514

leukodystrophy, hypomyelinating, 6MondoMONDO:0012905

leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadismMondoMONDO:0011897

leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadismMondoMONDO:0013722

leukodystrophy, hypomyelinating, 9MondoMONDO:0014506

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