Disease association ontology term - MONDO:0010516 - midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis

Term summary

ID: MONDO:0010516
Name: midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
Ontology or CV name: Disease association

Parents

is_a hereditary disease
is_a Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome

Annotation

Disease association

MONDO:0010516 - midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis

References:

PB_REF:0000006

Genes:

SPAC688.03c