Disease association ontology term - MONDO:0013659 - microcephaly-capillary malformation syndrome

Term summary

ID: MONDO:0013659
Name: microcephaly-capillary malformation syndrome
Ontology or CV name: Disease association

Parents

excluded_subClassOf obsolete obsolete rare capillary malformation with associated anomalies (obsolete MONDO:0018719)
is_a syndromic disease
is_a hereditary disease

Annotation

Disease association

MONDO:0013659 - microcephaly-capillary malformation syndrome

References:

PB_REF:0000006

Genes:

sst2 (SPAC19B12.10)