Search Ontology:
Human Disease

Nance-Horan syndrome

Term ID
DOID:0060599
Synonyms
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. (3)
References
Ontology
Human Disease   ( DOID:0060599 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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