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Intellectual deficit, X-linked, Raymond type
1 OMIM reference -
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
X-linked intellectual deficit with marfanoid habitus
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ZDHHC9 Q9Y397300646
No signs/symptoms info available.