Apodia




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Total: 1 (papers)

   


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
1
(60.5%)		 8072797
 [Oromandibular-limb hypogenesia spectrum: report of a case of lower ankylogloxia ++ associated with bilateral apodia].
Camera G, Camera A, Verrina G, Trasino S, Malvasio S.
Pathologica. 1994;86(1):110-2.
Micrognathia Ankyloglossia
Congenital Foot Deformity Homo sapiens Male
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 2

HPO ID Term # of case reports
HP:0000347 Micrognathia 1
HP:0010296 Ankyloglossia 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID