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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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Anatomy
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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

1,260 of 23,730 begin with H

hereditary spastic paraplegia 50MondoMONDO:0013048
hereditary spastic paraplegia 51MondoMONDO:0013401
hereditary spastic paraplegia 52MondoMONDO:0013552
hereditary spastic paraplegia 53MondoMONDO:0013962
hereditary spastic paraplegia 54MondoMONDO:0014018
hereditary spastic paraplegia 55

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

MondoMONDO:0014020

hereditary spastic paraplegia 56MondoMONDO:0014015

hereditary spastic paraplegia 57MondoMONDO:0014295

hereditary spastic paraplegia 5AMondoMONDO:0010047

hereditary spastic paraplegia 6MondoMONDO:0010878

hereditary spastic paraplegia 61MondoMONDO:0014304

hereditary spastic paraplegia 62MondoMONDO:0014302

hereditary spastic paraplegia 63MondoMONDO:0014305

hereditary spastic paraplegia 64MondoMONDO:0014303

hereditary spastic paraplegia 7MondoMONDO:0011803

hereditary spastic paraplegia 72MondoMONDO:0014282

hereditary spastic paraplegia 73MondoMONDO:0014568

hereditary spastic paraplegia 74MondoMONDO:0014644

hereditary spastic paraplegia 75MondoMONDO:0014729

hereditary spastic paraplegia 77MondoMONDO:0014882

hereditary spastic paraplegia 8MondoMONDO:0011339

hereditary spastic paraplegia 9AMondoMONDO:0011006

hereditary spherocytosisMondoMONDO:0019350

hereditary spherocytosis type 1MondoMONDO:0008447

hereditary spherocytosis type 2MondoMONDO:0000913

hereditary spherocytosis type 3MondoMONDO:0010053

hereditary spherocytosis type 4MondoMONDO:0012981

hereditary spherocytosis type 5MondoMONDO:0012985

hereditary stomatocytosisMondoMONDO:0020102

hereditary thermosensitive neuropathyMondoMONDO:0011197

hereditary thrombocytopenia and hematologic cancer predisposition syndromeMondoMONDO:0011071

hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1MondoMONDO:0100083

hereditary thrombocytosis with transverse limb defectMondoMONDO:0018000

hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiencyMondoMONDO:0013143

hereditary thrombophilia due to congenital protein C deficiencyMondoMONDO:0019145

hereditary thrombophilia due to congenital protein S deficiencyMondoMONDO:0019144

hereditary von Willebrand diseaseMondoMONDO:0019565

hereditary Wilms tumorMondoMONDO:0003321

hereditary xanthinuriaMondoMONDO:0018106

heritable pulmonary arterial hypertensionMondoMONDO:0017148

Hermansky-Pudlak syndromeMondoMONDO:0019312

Hermansky-Pudlak syndrome 1MondoMONDO:0008748

Hermansky-Pudlak syndrome 10MondoMONDO:0014885

Hermansky-Pudlak syndrome 11MondoMONDO:0030903

Hermansky-Pudlak syndrome 2MondoMONDO:0011997

Hermansky-Pudlak syndrome 3MondoMONDO:0013555

Hermansky-Pudlak syndrome 4MondoMONDO:0013556

Hermansky-Pudlak syndrome 5MondoMONDO:0013557

Hermansky-Pudlak syndrome 6MondoMONDO:0013558

Hermansky-Pudlak syndrome 7MondoMONDO:0013559

Hermansky-Pudlak syndrome 8MondoMONDO:0013560

Hermansky-Pudlak syndrome 9MondoMONDO:0013606

Hermansky-Pudlak syndrome with pulmonary fibrosisMondoMONDO:0016501

Hermansky-Pudlak syndrome without pulmonary fibrosisMondoMONDO:0016502

Hernández-Aguirre Negrete syndromeMondoMONDO:0016290

hernia, anterior diaphragmaticMondoMONDO:0010606

hernia, double inguinalMondoMONDO:0007720

heroin dependenceMondoMONDO:0005367

herpanginaMondoMONDO:0005791

herpes labialisMondoMONDO:0043653

herpes simplex dermatitisMondoMONDO:0004712

herpes simplex encephalitisMondoMONDO:0012521

herpes simplex encephalitis, susceptibility to, 1MondoMONDO:0024563

herpes simplex encephalitis, susceptibility to, 2MondoMONDO:0013075

herpes simplex encephalitis, susceptibility to, 3MondoMONDO:0013920

herpes simplex encephalitis, susceptibility to, 4MondoMONDO:0013921

herpes simplex encephalitis, susceptibility to, 7MondoMONDO:0014680

herpes simplex infectious diseaseMondoMONDO:0004609

herpes simplex type 1 infectious diseaseMondoMONDO:0100359

herpes simplex type 2 infectious diseaseMondoMONDO:0100360

herpes simplex virus gingivostomatitisMondoMONDO:0005792

herpes simplex virus keratitisMondoMONDO:0015288

herpes zosterMondoMONDO:0005609

herpes zoster dermatitisMondoMONDO:0021033

herpes zoster with dermatitis of eyelidMondoMONDO:0021032

Herpesviridae infectious diseaseMondoMONDO:0005794

herpetic gastritisMondoMONDO:0003769

herpetic vulvovaginitisMondoMONDO:0021175

herpetic whitlowMondoMONDO:0004616

herpetiform pemphigusMondoMONDO:0016164

heterochromia iridisMondoMONDO:0007722

heterophyiasisMondoMONDO:0004662

heterotaxy, visceral, 1, X-linkedMondoMONDO:0010607

heterotaxy, visceral, 10, autosomal, with male infertilityMondoMONDO:0030474

heterotaxy, visceral, 11, autosomal, with male infertilityMondoMONDO:0030475

heterotaxy, visceral, 12, autosomalMondoMONDO:0859222

heterotaxy, visceral, 13, autosomalMondoMONDO:0976134

heterotaxy, visceral, 14, autosomalMondoMONDO:0976135

heterotaxy, visceral, 2, autosomalMondoMONDO:0011546

heterotaxy, visceral, 3, autosomalMondoMONDO:0011659

heterotaxy, visceral, 4, autosomalMondoMONDO:0013403

heterotaxy, visceral, 5, autosomalMondoMONDO:0700112

heterotaxy, visceral, 6, autosomalMondoMONDO:0013887

heterotaxy, visceral, 7, autosomalMondoMONDO:0014762

heterotaxy, visceral, 8, autosomalMondoMONDO:0014967

heterotaxy, visceral, 9, autosomal, with male infertilityMondoMONDO:0030070

heterotopia, periventricular, associated with chromosome 5P anomaliesMondoMONDO:0011967

heterotopia, periventricular, X-linked dominantMondoMONDO:0010233

Heyn-Sproul-Jackson syndromeMondoMONDO:0032882

HGSNAT-related retinopathyMondoMONDO:1040040

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