Phenotypes for disease #03978 (MMDD (myopathy, due to myoadenylate deaminase deficiency (MMDD)), OMIM:615511)

1 entry on 1 page. Showing entry 1.
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     
0000106835 global developmental delay, muscular hypotonia, joint contractures (leg), no speech, hydrocephalus, cryptochism, CK elevation (2500 U/l) - - Unknown 08y 07y - - - Andreas Laner 00134082
Legend   How to query  


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