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N Syndrome (MONDO:0010686)

N syndrome is characterized by intellectual deficit, deafness, ocular anomalies, T-cell leukemia, cryptorchidism, hypospadias and spasticity.

Overview

Category

Ontology ID

Internal:11830

Synonyms

N syndrome

NSX

intellectual disability, malformations, chromosome breakage, and development of T-cell leukaemia

intellectual disability, malformations, chromosome breakage, and development of T-cell leukemia

mental retardation, malformations, chromosome breakage, and development of T-cell leukaemia

mental retardation, malformations, chromosome breakage, and development of T-cell leukemia

Mapped terms

DOID:0050769

GARD:0003902

MEDGEN:424834

MESH:C536108

OMIM:310465

Orphanet:2608

SCTID:723410002

UMLS:C2936859

icd11.foundation:2040480507

Child terms

Unknown children.