OBO ID: DOID:0060599
Term Name: Nance-Horan syndrome Search Ontology:
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 Nance-Horan syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NHS Nance-Horan syndrome 302350
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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