Disease association ontology term - MONDO:0054636 - Skraban-Deardorff syndrome
Term summary
ID
MONDO:0054636
Name
Skraban-Deardorff syndrome
Ontology or CV name
Disease association
Parents
is_a
syndromic disease
is_a
hereditary disease
is_a
multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Annotation
Disease association
MONDO:0054636
-
Skraban-Deardorff syndrome
References:
PB_REF:0000006
Genes:
gid7 (SPAC343.04c)