Fibular dimelia-diplopodia syndrome

Fibular dimelia-diplopodia syndrome is a rare developmental anomaly.



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Total: 0 (papers)
  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 3

HPO ID Term Frequency
HP:0009556 Absent tibia Very frequent (99-80%)
HP:0000271 Abnormality of the face Frequent (79-30%)
HP:0030736 Sacrococcygeal teratoma Frequent (79-30%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID