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N syndrome

Disease Summary
Associated Targets (1)
Tclin

1


GARD Rare
Mondo Description N syndrome is characterised by intellectual deficit, deafness, ocular anomalies, T-cell leukaemia, cryptorchidism, hypospadias and spasticity.
Mondo Term and Equivalent IDs
MONDO:0010686:  N syndrome
DOID:0050769: N syndrome
GARD:0003902: 
MESH:C536108: 
OMIM:310465: N SYNDROME
Orphanet:2608: 
SCTID:723410002: 
UMLS:C2936859: