Phenotypes for disease #00844 (MPPH1 (megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome, type 1 (MPPH-1)), OMIM:603387)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000042699 MPPH syndrome - - Isolated (sporadic) - - - - - Norine Voisin 00034521
0000042702 mild developmental delay particularly involving speech, later diagnosed with Asperger syndrome; 18m-third ventriculostomy for progressive ventriculomegaly (HP:0002119), no seizures; 12.5y MRI-brain striking megalencephaly (HP:0001355), bilateral perisylvian polymicrogyria (HP:0002126), borderline cerebellar tonsillar ectopia, moderately thick corpus callosum, no vascular malformations, no digital anomalies (no polydactyly (-HP:0010442), no syndactyly (-HP:0001159)) - - Familial 16y - - ventriculomegaly (HP:0002119) - Johan den Dunnen 00056046
0000350535 Intellectual disability, Macrocephaly, Seizure, Neurodevelopmental delay - - Isolated (sporadic) 17y - - - - Andreas Laner 00464536
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