Phenotypes for disease #03585 (HPE11 (holoprosencephaly, type 11 (HPE-11)), OMIM:614226)

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000093192 agenesis of corpus callosum, hypotelorism, growth hormone deficiency, global developmental delay; dark, thick eyebrows with synophrys - - Unknown - - - - - Johan den Dunnen 00117727
0000093193 suspected autosomal dominant HPE, microcephaly, developmental delay - - Unknown - - - - - Johan den Dunnen 00117728
0000093194 HPE-like, midline cyst of falx cerebri - - Unknown - - - - - Johan den Dunnen 00117729
0000093195 agenesis of corpus callosum, alobar HPE, hypotelorism, mild proptosis, median cleft lip/palate, absent columella, cryptochidism - - Unknown - - - - - Johan den Dunnen 00117730
0000093196 alobar HPE findings - - Unknown - - - - - Johan den Dunnen 00117731
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.