Phenotypes for disease #04139 (MPPH2 (megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome, type 2 (MPPH-2)), OMIM:615937)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000042701 2y5m OFC +6; no overgrowth (-HP:0001548), no asymmetry, no vascular malformations, no polydactyly (-HP:0010442), no syndactyly (-HP:0001159), connective tissue dysplasia (skin laxity, joint hypermobility, thick doughy subcutaneous tissue), hydrocephalus (HP:0000238), ventriculomegaly (HP:0002119), no cerebellar tonsillar ectopia, polymicrogyria (HP:0002126) - - Isolated (sporadic) 02y05m - - - - Johan den Dunnen 00056045
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