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Microcephalic primordial dwarfism due to ZNF335 deficiency
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal recessive primary microcephaly
Dedifferentiated liposarcoma
Familial melanoma
Well-differentiated liposarcoma
Methylmalonic acidemia with homocystinuria, type cblX
X-linked non-syndromic intellectual deficit
- Microcephalic primordial dwarfism, Walsh type

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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
ZNF335 Q9H4Z2610827
No signs/symptoms info available.