Phenotypes for disease #01654 (ALS2 (sclerosis, lateral, amyotrophic, type type 2 (ALS2)), OMIM:205100)

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     
0000367337 marked intellectual disability, cognitive impairment, mild microcephaly, and spasticity of both upper and lower limbs; language impairment, delayed milestones, bilateral foot drop, dysarthria, swallowing difficulties amyotrophic lateral sclerosis - Familial, autosomal recessive 20y 20y - - - Atta Ur Rehman 00484548
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.