Phenotypes for disease #05242 (HGPPS2 (gaze palsy, horizontal, with progressive scoliosis, type-2), OMIM:617542)

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000079578 Agenesis of the corpus callosum. Absence of anterior and hippocampal commissures. Hypoplastic pons and midbrain. Midline cleft of the brainstem. Global motor delay, horizontal gaze palsy, intellectual disability, scoliosis. - - Familial, autosomal recessive - - - - Ashley Marsh 00101374
0000079579 Agenesis of the corpus callosum. Absence of anterior and hippocampal commissures. Hypoplastic pons and midbrain. Midline cleft of the brainstem. Horizontal gaze palsy, intellectual disability, progressive scoliosis, global developmental delay, hypotonia. Mirror movements. - - Familial, autosomal recessive - - - - Ashley Marsh 00101210
0000079581 Agenesis of the corpus callosum. Absence of anterior and hippocampal commissures. Hypoplastic pons and midbrain. Midline cleft of the brainstem. Horizontal gaze palsy, intellectual disability, progressive scoliosis, global developmental delay, hypotonia, short stature. Mirror movements. - - Familial, autosomal recessive - - - - Ashley Marsh 00101209
Legend   How to query  


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