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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Intermittent hydrarthrosis
Microcephaly-capillary malformation syndrome

MEFV STAMBP
TNFRSF1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TNFRSF1A
(0.52)
STAMBP



Citations in the biomedical literature:


Intermittent hydrarthrosis
MEFV TNFRSF1A
Microcephaly-capillary malformation syndrome
STAMBP



Intermittent hydrarthrosis
Microcephaly-capillary malformation syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- MIC-CAP syndrome
- MIC-CM syndrome
- Microcephaly-cutaneous capillary malformation syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.