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CLN1 disease
1 OMIM reference -
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Dedifferentiated liposarcoma
Familial multiple nevi flammei
Sturge-Weber syndrome
Well-differentiated liposarcoma
5p13 microduplication syndrome
Cornelia de Lange syndrome
Sanfilippo syndrome type A
Treacher-Collins syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
PPT1 P50897600722
No signs/symptoms info available.