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Tessier number 4 facial cleft
1 OMIM reference -
1 associated gene
9 connected diseases
No signs/symptoms info
Disease Type of connection
Commissural facial cleft
APC-related attenuated familial adenomatous polyposis
Acute megakaryoblastic leukemia without Down syndrome
Desmoid tumor
Familial adenomatous polyposis due to 5q22.2 microdeletion
Gardner syndrome
Juvenile autosomal recessive medullary cystic kidney disease
Papillary or follicular thyroid carcinoma
Turcot syndrome with polyposis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SPECC1L Q69YQ0614140
No signs/symptoms info available.