Phenotypes for disease #03907 (LGMDR18;LGMD2S (dystrophy, muscular, limb-girdle, autosomal recessive, type 18 (LGMD2S)), OMIM:615356)

2 entries on 1 page. Showing entries 1 - 2.
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     
0000087489 Strabismus, mildly elevated CK, moderate ID, movement disorder - - Familial, autosomal recessive - - - - - Bernt Popp 00111404
0000094091 early onset limb girdle muscular dystrophy (HP:0006785); walk-22m, muscular pseudohypertrophy (HP:0003707), proximal weakness (HP:0003701), bilateral cataracts (HP:0000519), normal cognition (no ntellectual disability, HP:0001249) - - Familial, autosomal recessive 05y 03y 01y - - Nadine McCrea 00119098
Legend   How to query  


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