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Familial cortical myoclonus
1 OMIM reference -
1 associated gene
17 connected diseases
No signs/symptoms info
Disease Type of connection
B-cell chronic lymphocytic leukemia
Autoimmune lymphoproliferative syndrome with recurrent infections
Microcephaly - seizures - developmental delay
Adrenocortical carcinoma
Dyskeratosis congenita
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Hereditary cerebral cavernous malformation
Hoyeraal-Hreidarsson syndrome
Li-Fraumeni syndrome
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Retinopathy - anemia- central nervous system anomalies
FADD-related immunodeficiency
Oculootodental syndrome
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
NOL3 O60936605235
No signs/symptoms info available.