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3M syndrome 1 | RareConnect | RareConnect.io

/primordial dwarfism and slender bone disorder

/3M syndrome 1

3M syndrome 1

Rare Disease

MONDO:0010117

Also Known As

3-M syndrome 13-M syndrome caused by mutation in CUL73-M syndrome caused by mutation in Cul7CUL7 3-M syndromeCul7 3-M syndromethree M syndrome 1three M syndrome type 13M syndrome3M1Dolichospondylic dysplasiaLe Merrer syndromeYakut short stature syndromegloomy face syndrome

Definition

Any 3-M syndrome in which the cause of the disease is a mutation in the CUL7 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:273750 ↗

GARD

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