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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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Reach

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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

175 of 23,730 begin with X

X-linked Mendelian susceptibility to mycobacterial diseasesMondoMONDO:0017905
X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiencyMondoMONDO:0010389
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndromeMondoMONDO:0018569
X-linked mixed hearing loss with perilymphatic gusherMondoMONDO:0010576
X-linked myopathy with excessive autophagyMondoMONDO:0010684

More of the reference layer

Pathways
Biological processes
Anatomy
Cell types
Organisms
Materials
Regulatory assessments

Evidence: Compounds · Outcomes · Papers · Search

X-linked myopathy with postural muscle atrophyMondoMONDO:0010401

X-linked myotubular myopathyMondoMONDO:0010683

X-linked myotubular myopathy-abnormal genitalia syndromeMondoMONDO:0010271

X-linked neurodegenerative syndrome, Bertini typeMondoMONDO:0019427

X-linked neurodegenerative syndrome, Hamel typeMondoMONDO:0019429

X-linked non progressive cerebellar ataxiaMondoMONDO:0010404

X-linked nonsyndromic hearing lossMondoMONDO:0019586

X-linked Opitz G/BBB syndromeMondoMONDO:0010222

X-linked osteoporosis with fracturesMondoMONDO:0018315

X-linked parkinsonism-spasticity syndromeMondoMONDO:0010482

X-linked progressive cerebellar ataxiaMondoMONDO:0010547

X-linked recessive diseaseMondoMONDO:0020605

X-linked recessive mitochondrial myopathyMondoMONDO:0100138

X-linked recessive ocular albinismMondoMONDO:0021019

X-linked reticulate pigmentary disorderMondoMONDO:0010523

X-linked retinal dysplasiaMondoMONDO:0010722

X-linked retinoschisisMondoMONDO:0010725

X-linked scapuloperoneal muscular dystrophyMondoMONDO:0010400

X-linked severe congenital neutropeniaMondoMONDO:0010294

X-linked severe syndromic thoracic aortic aneurysm and dissectionMondoMONDO:0850095

X-linked sideroblastic anemia 1MondoMONDO:0020721

X-linked sideroblastic anemia with ataxiaMondoMONDO:0010524

X-linked spasticity-intellectual disability-epilepsy syndromeMondoMONDO:0017856

X-linked spermatogenic failure 1MondoMONDO:0056795

X-linked spinocerebellar ataxia type 3MondoMONDO:0010529

X-linked spinocerebellar ataxia type 4MondoMONDO:0010534

X-linked spondyloepimetaphyseal dysplasiaMondoMONDO:0010248

X-linked syndromic complex neurodevelopmental disorderMondoMONDO:1040018

X-linked syndromic intellectual disabilityMondoMONDO:0020119

xanthinuriaMondoMONDO:0000721

xanthinuria type IMondoMONDO:0010209

xanthinuria type IIMondoMONDO:0011346

xanthogranulomaMondoMONDO:0024617

xanthogranulomatous cholecystitisMondoMONDO:0004875

xanthogranulomatous hypophysitisMondoMONDO:1060218

xanthogranulomatous pyelonephritisMondoMONDO:0007022

xanthogranulomatous sialadenitisMondoMONDO:0027091

xanthomaMondoMONDO:0005236

xanthoma disseminatumMondoMONDO:0015535

xanthomatosisMondoMONDO:0002615

xanthomatosis, susceptibility toMondoMONDO:0011207

xanthomatous hypophysitisMondoMONDO:1060217

xeroderma of eyelidMondoMONDO:0004718

xeroderma pigmentosumMondoMONDO:0019600

xeroderma pigmentosum group AMondoMONDO:0010210

xeroderma pigmentosum group BMondoMONDO:0012531

xeroderma pigmentosum group CMondoMONDO:0010211

xeroderma pigmentosum group DMondoMONDO:0010212

xeroderma pigmentosum group EMondoMONDO:0010213

xeroderma pigmentosum group FMondoMONDO:0010215

xeroderma pigmentosum group GMondoMONDO:0010216

xeroderma pigmentosum variant typeMondoMONDO:0010214

xeroderma pigmentosum-Cockayne syndrome complexMondoMONDO:0016354

xeroderma pigmentosum, autosomal dominant, mildMondoMONDO:0008690

xeroderma pigmentosum, complementation group JMondoMONDO:0980987

xeroderma pigmentosum, type F/Cockayne syndromeMondoMONDO:0800313

xeroderma pigmentosum, type G/Cockayne syndromeMondoMONDO:0800314

xerophthalmiaMondoMONDO:0000948

xerosis and growth failure with immune and pulmonary dysfunction syndromeMondoMONDO:0957786

XFE progeroid syndromeMondoMONDO:0012590

XK aprosencephalyMondoMONDO:0008811

XK-related neurodegenerative diseaseMondoMONDO:0018945

Xp22.13p22.2 duplication syndromeMondoMONDO:0017284

Xp22.3 microdeletion syndromeMondoMONDO:0015606

Xq12-q13.3 duplication syndromeMondoMONDO:0017794

Xq25 microduplication syndromeMondoMONDO:0010507

Xq27.3q28 duplication syndromeMondoMONDO:0010467

XY type gonadal dysgenesis-associated anomalies syndromeMondoMONDO:0009302

xylosidase deficiencyMondoMONDO:0010219

XYLT1-congenital disorder of glycosylationMondoMONDO:0018273

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