Phenotypes for disease #00181 (CMYO6;MYPOP (myopathy, congenital, type 6, with ophthalmoplegia), OMIM:605637)

11 entries on 1 page. Showing entries 1 - 11.
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     
0000001830 autosomal dominant inclusion body myopathy, joint contractures, ophthalmoplegia, rimmed vacuoles - - Familial, autosomal dominant - - - - - Johan den Dunnen 00002674
0000001831 pronounced opthalmoplegia; ptosis; ... - - Isolated (sporadic) 41y - - - - Homa Tajsharghi 00002919
0000001832 pronounced opthalmoplegia; no ptosis; ... - - Isolated (sporadic) 42y - - - - Homa Tajsharghi 00002920
0000001833 pronounced opthalmoplegia; no ptosis; ... - - Isolated (sporadic) 44y - - - - Homa Tajsharghi 00002921
0000001834 pronounced opthalmoplegia; no ptosis; ... - - Isolated (sporadic) 58y - - - - Homa Tajsharghi 00002925
0000001835 pronounced opthalmoplegia; ptosis; ... - - Isolated (sporadic) 59y - - - - Homa Tajsharghi 00002928
0000001836 external ophthalmoplegia; conjugate non-restrictive ocular motility impairment, no ptosis, mild facial/limb muscle weakness, scoliosis; skeletal muscle biopsy marked type 1 fibre predominance - - Familial, autosomal recessive - - - - - Homa Tajsharghi 00002929
0000001837 - - - Familial, autosomal recessive - - - - - Homa Tajsharghi 00002930
0000001838 - - - Familial, autosomal recessive - - - - - Homa Tajsharghi 00002931
0000001839 - - - Familial, autosomal recessive - - - - - Homa Tajsharghi 00002933
0000325387 Axial muscle weakness, Skeletal muscle atrophy, Motor delay, Poor suck, Difficulty descending stairs, Strabismus - - Familial, autosomal recessive 07y - - - - Andreas Laner 00435182
Legend   How to query  


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