Disease association ontology term - MONDO:0007785 - hyperthyroxinemia, dystransthyretinemic

Term summary

ID: MONDO:0007785
Name: hyperthyroxinemia, dystransthyretinemic
Ontology or CV name: Disease association

Parents

is_a hereditary disease
is_a hyperthyroxinemia

Annotation

Disease association

MONDO:0007785 - hyperthyroxinemia, dystransthyretinemic

References:

PB_REF:0000006

Genes:

SPCC285.04