N syndrome

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: pola1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010686 - manual digit phalanx cartilage element

MONDO:0010686 - manual digit phalanx cartilage element

MIM:

MIM:310465 - N SYNDROME; NSX

MIM:310465 - N SYNDROME; NSX

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): syndrome (is_a)