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Disease Ontology Browser
Nance-Horan syndrome (DOID:0060599)
Alliance: disease page
Alt IDs: OMIM:302350, ICD10CM:Q87.0, MESH:C538336, ORDO:627, UMLS_CUI:C0796085
Definition: An X-linked disease that has_material_basis_in mutation in the NHS gene on chromosome Xp22. It is characterized by congenital cataract leading to profound vision loss, characteristic dysmorphic features and dental anomalies.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory