Phenotypes for disease #03124 (MRD22;del1q43q44 (mental retardation, autosomal dominant, type 22 (MRD22, 1q43-q44 deletion syndrome)), OMIM:612337)

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     
0000279599 Intellectual disability, Hearing impairment, Seizure, Delayed speech and language development, Hypoplasia of the corpus callosum - - Isolated (sporadic) 12y - - - - Andreas Laner 00385789
Legend   How to query  


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