Phenotypes for disease #06256 (ALS5 (Amyotrophic lateral sclerosis 5, juvenile), OMIM:602099)

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000357438 neurodevelopmental disorder CDG2J severe intellectual disability, spasticity, absent speech, microcephaly, neuromotor delay Familial, autosomal recessive - - - - Lucia Micale 00472642
Legend   How to query  


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