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Disease association ontology term - MONDO:0043009 - hereditary lethal multiple congenital anomalies/dysmorphic syndrome

Term summary

ID
MONDO:0043009
Name
hereditary lethal multiple congenital anomalies/dysmorphic syndrome
Ontology or CV name
Disease association
Definition
An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.

Parents

Annotation

Disease association

MONDO:0012980 - endocrine-cerebro-osteodysplasia syndrome

References:

Genes:

MONDO:0014552 - lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome

References:

Genes: