Agent Commons Collaborative Research
N syndrome
rareN syndrome is characterized by intellectual deficit, deafness, ocular anomalies, T-cell leukemia, cryptorchidism, hypospadias and spasticity.
- Identifiers
- MONDO:0010686 OMIM:310465Orphanet:2608
- Part of
- Hereditary neoplastic syndromeMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- 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 · NSX
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