Disease association ontology term - MONDO:0033642 - neurodevelopmental disorder with alopecia and brain abnormalities

Term summary

ID: MONDO:0033642
Name: neurodevelopmental disorder with alopecia and brain abnormalities
Ontology or CV name: Disease association

Parents

excluded_subClassOf inborn disorder of ornithine metabolism
is_a Mendelian neurodevelopmental disorder
is_a disorder of polyamine metabolism

Annotation

Disease association

MONDO:0033642 - neurodevelopmental disorder with alopecia and brain abnormalities

References:

PB_REF:0000006

Genes:

spe1 (SPAC144.04c)