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3-M syndrome

Disease Summary
Associated Targets (3)
Tbio

3


Explore Associated Targets
Mondo Description 3M syndrome is a primordial growth disorder characterized by low birth weight, reduced birth length, severe postnatal growth restriction, a spectrum of minor anomalies (including facial dysmorphism) and normal intelligence.
Disease Ontology Description An autosomal recessive disease characterized by dwarfism, facial dysmorphia and skeletal abnormalities.
Mondo Term and Equivalent IDs
MONDO:0007477:  3-M syndrome
GARD:0005667: 
MESH:C535314: 
OMIMPS:273750: 
Orphanet:2616: 
SCTID:702342007: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)