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1.

Van der Woude syndrome 2

Van der Woude syndrome (VWS) is a dominantly inherited developmental disorder characterized by pits and/or sinuses of the lower lip, and cleft lip and/or cleft palate (CL/P, CP). It is the most common cleft syndrome. For a discussion of genetic heterogeneity of van der Woude syndrome, see VWS1 (119300). [from OMIM]

MedGen UID:
338272
Concept ID:
C1847604
Disease or Syndrome
2.

Curry-Jones syndrome

Curry-Jones syndrome (CRJS) is a multisystem disorder characterized by patchy skin lesions, polysyndactyly, diverse cerebral malformations, unicoronal craniosynostosis, iris colobomas, microphthalmia, and intestinal malrotation with myofibromas or hamartomas (summary by Twigg et al., 2016). [from OMIM]

MedGen UID:
167083
Concept ID:
C0795915
Disease or Syndrome
3.

Lip pit

A depression located on a lip. [from HPO]

MedGen UID:
87412
Concept ID:
C0341059
Anatomical Abnormality
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