TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations

MONDO:1040001

Any developmental defect during embryogenesis in which the cause of the disease is a mutation in the TP63 gene. This disease is characterized by variable ectodermal dysplasia, limb defects, and orofacial clefting.

0 clinical trials for this condition and its sub-types, 0 tagged with TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations itself.

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↑ Hereditary disease (18235) ↑ Developmental defect during embryogenesis (1060)

Sub-types of TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations

ADULT syndrome 0 trials
Rapp-Hodgkin syndrome 0 trials
Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 0 trials
1 sub-type
- Rosselli-Gulienetti syndrome 0 trials
Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 0 trials
Split hand-foot malformation 4 0 trials

Including sub-types (0) Tagged with TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations (0)

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