Seckel syndrome 2

MONDO:0011715

Any Seckel syndrome in which the cause of the disease is a mutation in the RBBP8 gene.

Also known as: RBBP8 Seckel syndrome, SCKL2, Seckel syndrome 2, Seckel syndrome caused by mutation in RBBP8, Seckel syndrome type 2, Seckel-type dwarfism 2, microcephalic primordial dwarfism 2

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

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Part of

↑ Primordial dwarfism and slender bone disorder (9) ↑ Seckel syndrome (1)

Including sub-types (0) Tagged with Seckel syndrome 2 (0)

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