help  | about  | cite  | software

Disease :

Primary Identifier  OMIM:300519 Name  MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE
Quick Links:
 
Quick Links:
 

Genomics

0 Genes

Disease

Disease --> HPO phenotype terms

Disease --> alleles

 

Other

3 Data Sets

2 Publications