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Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
CLN3 disease
Fatal infantile cytochrome C oxidase deficiency
Leigh syndrome with cardiomyopathy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SFXN4 Q6P4A7615564
No signs/symptoms info available.