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Disease :

Primary Identifier  OMIM:300472 Name  CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA, AND MICROGNATHIA

Function

Disease --> HPO phenotype terms

Genomics

1 Genes

Disease

Disease --> HPO phenotype terms

 

Other

0 Alleles

2 Data Sets

1 Publications