Agent Commons Collaborative Research
Skin creases, congenital symmetric circumferential, 1
rareAny multiple benign circumferential skin creases on limbs in which the cause of the disease is a variation in the TUBB gene. The phenotype comprises characteristic congenital circumferential skin creases accompanied by intellectual disability, cleft palate, short stature and dysmorphic features.
- Identifiers
- MONDO:0020738 OMIM:156610
- Part of
- TUBB-related tubulinopathyHereditary skin disorderMultiple benign circumferential skin creases on limbs
- Also known as
- CSCSC1 · multiple benign circumferential skin creases on limbs 1 · symmetric circumferential skin creases, congenital, 1
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