Phenotypes for disease #00218 (IBMPFD1 (myopathy, inclusion body, with early-onset Paget disease and frontotemporal dementia, type 1), OMIM:167320)

20 entries on 1 page. Showing entries 1 - 20.
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     
0000001869 hereditary spastic paraplegia hereditary spastic paraplegia IBMPFD Isolated (sporadic) - - 06y - - Marcel Nelen 00003018
0000119163 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146423
0000119164 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146424
0000119165 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146425
0000119166 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146426
0000119167 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146427
0000119168 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146428
0000119169 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146429
0000119170 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146430
0000119171 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146431
0000119172 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146432
0000119173 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146433
0000119174 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146434
0000119175 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146435
0000119176 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146436
0000119177 no frontotemporal dementia(>60y) - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146437
0000119178 clinical heterogeneity and variable penetrance - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146438
0000119179 clinical heterogeneity and variable penetrance - - Familial, autosomal dominant - - - - - Johan den Dunnen 00146439
0000119184 able to walk, CPK 714 IU/l - - Unknown - 53y 48y - - Shiro Matsubara 00146444
0000271348 Muscle weakness, Achilles tendon contracture, Scapuloperoneal weakness, Abnormality of the Achilles tendon, Contractures involving the joints of the feet, Family history, Past medical history - - Familial, autosomal dominant - 62y - - - Andreas Laner 00376137
Legend   How to query  


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