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

Xenbase Genes : trim37

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009664 - 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)