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Summary Literature (0)
DOID:0050769 - N syndrome

Disease Ontology Definition:A syndrome that is characterized by intellectual disability, deafness, ocular abnormalities, T-cell leukemia, cryptorchidism, hypospadias and spasticity.

Synonyms: NSX

Xenbase Genes : pola1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010686 - manual digit phalanx cartilage element

MIM:
MIM:310465 - N SYNDROME; NSX

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): syndrome (is_a)