Triopia




Input patient's signs and symptoms


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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: 18

HPO ID Term Frequency
HP:0000161 Median cleft lip Very frequent (99-80%)
HP:0000175 Cleft palate Very frequent (99-80%)
HP:0000235 Abnormality of the fontanelles or cranial sutures Very frequent (99-80%)
HP:0000256 Macrocephaly Very frequent (99-80%)
HP:0000268 Dolichocephaly Very frequent (99-80%)
HP:0000316 Hypertelorism Very frequent (99-80%)
HP:0000324 Facial asymmetry Very frequent (99-80%)
HP:0000482 Microcornea Very frequent (99-80%)
HP:0000534 Abnormal eyebrow morphology Very frequent (99-80%)
HP:0000581 Blepharophimosis Very frequent (99-80%)
HP:0000612 Iris coloboma Very frequent (99-80%)
HP:0000615 Abnormal pupil morphology Very frequent (99-80%)
HP:0000951 Abnormality of the skin Very frequent (99-80%)
HP:0001561 Polyhydramnios Very frequent (99-80%)
HP:0001601 Laryngomalacia Very frequent (99-80%)
HP:0002007 Frontal bossing Very frequent (99-80%)
HP:0002084 Encephalocele Very frequent (99-80%)
HP:0100629 Midline facial cleft Very frequent (99-80%)


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