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Intellectual deficit, X-linked, Nascimento type
1 OMIM reference -
1 associated gene
30 connected diseases
No signs/symptoms info
Disease Type of connection
Familial pancreatic carcinoma
Precursor B-cell acute lymphoblastic leukemia
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
X-linked distal arthrogryposis multiplex congenita
Familial melanoma
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Precursor T-cell acute lymphoblastic leukemia
Familial prostate cancer
Hereditary breast and ovarian cancer syndrome
Johanson-Blizzard syndrome
Nijmegen breakage syndrome
Papillary or follicular thyroid carcinoma
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Hyperparathyroidism - jaw tumor syndrome
Infantile Refsum disease
Neonatal adrenoleukodystrophy
Parathyroid carcinoma
Zellweger syndrome
Amyotrophic lateral sclerosis
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
Synonym(s):
- X-linked intellectual deficit - nail dystrophy - seizures
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
UBE2A P49459312180
No signs/symptoms info available.