Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0050436 - mulibrey nanism

Disease Ontology Definition:A syndrome that is characterized by global growth retardation of the muscle, liver, brain and eyes as well as constrictive pericarditis and has_material_basis_in mutations in the TRIM37 gene.

Synonyms: Muscle-Liver-Brain-Eye Nanism, Perheentupa Syndrome, PERICARDIAL CONSTRICTION AND GROWTH FAILURE, MUL, Mulibrey growth disorder

Echinobase Genes : trim37


MIM:
MIM:253250 - mulibrey nanism

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)