Phenotypes for disease #03702 (PCH1B (hypoplasia, pontocerebellar, type 1b (PCH-1B)), OMIM:614678)

14 entries on 1 page. Showing entries 1 - 14.
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     
0000085596 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 08m - - - - Johan den Dunnen 00107835
0000085597 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 08m - - - - Johan den Dunnen 00107836
0000085598 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 17m - - - - Johan den Dunnen 00107837
0000085599 Pontocerebellar hypoplasia type 1 (PCH1), seen at 3m - - Familial, autosomal recessive 03m - - - - Johan den Dunnen 00107838
0000085600 floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 18y - - - - Johan den Dunnen 00107839
0000085601 floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 18y - - - - Johan den Dunnen 00107840
0000085602 floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 16y - - - - Johan den Dunnen 00107841
0000085603 floppy at birth; ocular motor apraxia; progressive muscle wasting, distal contractures; progressive microcephaly; growth retardation; global developmental delay; never reached any motor milestone or spoke; Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 09y - - - - Johan den Dunnen 00107842
0000085604 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 40m - - - - Johan den Dunnen 00107843
0000085605 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 20y - - - - Johan den Dunnen 00107844
0000085606 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 16y - - - - Johan den Dunnen 00107845
0000085607 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 26m - - - - Johan den Dunnen 00107846
0000085608 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 03y - - - - Johan den Dunnen 00107847
0000085609 Pontocerebellar hypoplasia type 1 (PCH1) - - Familial, autosomal recessive 11m - - - - Johan den Dunnen 00107848
Legend   How to query  


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