help  | about  | cite  | software

Disease :

Primary Identifier  OMIM:309583 Name  MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE

Function

Disease --> HPO phenotype terms

Genomics

1 Genes

Disease

Disease --> HPO phenotype terms

 

Other

10 Alleles

3 Data Sets

8 Publications