Disease association ontology term - MONDO:0035819 - cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome

Term summary

ID: MONDO:0035819
Name: cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome
Ontology or CV name: Disease association

Parents

is_a syndromic disease
is_a hereditary disease

Annotation

Disease association

MONDO:0035819 - cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome

References:

PB_REF:0000006

Genes:

vps4 (SPAC2G11.06)