3M syndrome 2

MONDO:0013039

Any 3-M syndrome in which the cause of the disease is a mutation in the OBSL1 gene.

Also known as: 3-M syndrome 2, 3-M syndrome caused by mutation in OBSL1, 3M syndrome 2, OBSL1 3-M syndrome, three M syndrome 2, three M syndrome type 2, 3M2

0 clinical trials for this condition and its sub-types, 0 tagged with 3M syndrome 2 itself.

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Part of

↑ Primordial dwarfism and slender bone disorder (9) ↑ 3-M syndrome (0)

Including sub-types (0) Tagged with 3M syndrome 2 (0)

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