Phenotypes for disease #00319 (PCH6 (hypoplasia, pontocerebellar, type 6 (PCH-6)), OMIM:611523)

7 entries on 1 page. Showing entries 1 - 7.
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Phenotype details     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000003238 neonatal lactic acidosis, hypotonia, developmental delay, seizures, cortical atrophy, pontocerebellar hypoplasia on MRI - - Unknown - - - - - Carl Fratter 00004531
0000003239 neonatal lactic acidosis, developmental delay, microcephaly, cortical atrophy, pontocerebellar hypoplasia on MRI - - Unknown - - - - - Carl Fratter 00004532
0000174479 severe developmental delay, seizures, microcephaly PEHO syndrome PCH6 Familial, autosomal recessive - - - - - Carolina Courage 00234052
0000232681 neurodevelopmental delay. myoclonic seizures, , axial hypotonia with distal hypertonia, microcephaly, mixed hearing loss, abnormal breathing pattern, cryptorchidism - - Isolated (sporadic) 00y06m - - - - Enza Maria Valente 00306853
0000257408 Sibling -pair with childhood onset mild progressive ataxia, mild predominantly upper limb action myoclonus, occasional TCS and absence seizures. Childhood onset cognitive impairment diagnosed prior to onset of myoclonus and ataxia. MRI unremarkable. progressive myoclonus epilepsy , dementia - Familial, autosomal recessive - - - - - Johan den Dunnen 00334933
0000257409 see sib progressive myoclonus epilepsy , dementia - Familial, autosomal recessive - - - - - Johan den Dunnen 00334935
0000257410 Onset 25 years of prominent progressive action myoclonus. Normal developmental history, normal cognition. No ataxia, no TCS. Scoliosis and ovarian insufficiency. late onset progressive myoclonus epilepsy - Familial, autosomal recessive - - - - - Johan den Dunnen 00334936
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