FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term mulibrey nanism ID (Ontology) DOID:0050436 (Human Disease)
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.
Also Known As "MUL" ; "Mulibrey growth disorder" ; "Muscle-Liver-Brain-Eye Nanism" (for all, see Synonyms field below)
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Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__syndrome_____________________|
                                 mulibrey nanism
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Is a autosomal recessive disease
syndrome
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Synonyms
  • "MUL" EXACT OMO:0003012
    "Mulibrey growth disorder" EXACT
    "Muscle-Liver-Brain-Eye Nanism" EXACT
    "Perheentupa Syndrome" EXACT
    "PERICARDIAL CONSTRICTION AND GROWTH FAILURE" EXACT
Secondary IDs
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GARD:95
MESH:D050336
MIM:253250
NCI:C84906
ORDO:2576
SNOMEDCT_US_2023_03_01:81604003
UMLS_CUI:C0524582