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Summary Literature (0)
DOID:0060599 - Nance-Horan syndrome

Disease Ontology Definition:A syndrome that has_material_basis_in mutation in the NHS gene on chromosome Xp22 and is characterized by congenital cataract leading to profound vision loss, characteristic dysmorphic features and dental anomalies.

Synonyms:

Xenbase Genes : nhs

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010545 - Nance-Horan syndrome


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): X-linked monogenic disease (is_a), syndrome (is_a)