FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term 3-M syndrome ID (Ontology) DOID:0060241 (Human Disease)
Definition A syndrome characterized by dwarfism, facial dysmorphia and skeletal abnormalities.
Also Known As "dolichospondylic dysplasia" ; "gloomy face syndrome" ; "Le Merrer syndrome" (for all, see Synonyms field below)
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 Genes
 3-M syndrome       3
 for disease ribbon | 3-M syndrome       3
 model of | 3-M syndrome       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__syndrome_____________________|
                                 3-M syndrome  3 rec.
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Is a autosomal recessive disease
syndrome
Part of
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Synonyms
  • "dolichospondylic dysplasia" EXACT
    "gloomy face syndrome" EXACT
    "Le Merrer syndrome" EXACT
    "Miller-McKusick-Malvaux syndrome" EXACT
    "three M syndrome" EXACT
    "Yakut short stature syndrome" EXACT
Secondary IDs
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GARD:5667
MESH:C535314
MIM:273750
MIM:612921
MIM:614205
ORDO:2616
SNOMEDCT_US_2023_03_01:702342007
UMLS_CUI:C1848862
UMLS_CUI:C3280146