Pharos : Disease Details - Nuchal bleb, familial

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Nuchal bleb, familial

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Disease Summary

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Download Data for Nuchal bleb, familial

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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.

DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.

High level summary of knowledge for a disease, including descriptions and datasource references.

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Opens the Target List with this set of targets

Download Data for mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency

This disease has been annotated by GARD as a rare disease.

Description from Mondo Disease Ontology.

GARD:0003011

MESH:C535530

Orphanet:99898

UMLS:C2930924

MONDO:0020530