Pai syndrome
Median cleft of the upper lip-corpus callosum lipoma-cutaneous polyps syndrome
Facts
5 properties- Instance of
- class of disease
- Subclass of
- midface dysplasia, orofacial clefting syndrome, developmental defect during embryogenesis, head and neck disease
- Has phenotype
- Median cleft upper lip, cleft palate, skin tag, nasal polyps, bifid uvula, hypertelorism, telecanthus, coloboma of iris, encephalocele[9][10][11][12][13][14][15][16][17]
- Prevalence
- +0.000001[6]
🏷️ Also known as
en CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA
en Median cleft of the upper lip-corpus callosum lipoma-cutaneous polyps syndrome
en Median cleft of upper lip with polyps of facial skin and nasal mucosa
en Pai syndrome
fr syndrome de Pai
🔖 Identifiers · 10
- Exact match
- www.orpha.net
- GARD rare disease ID
- 3439
- ICD-10-CM
- Q87.8
- ICD-11 ID (Foundation)
- 1236130516
- MeSH descriptor ID
- C536135
- Mondo ID
- MONDO_0007956
- OMIM ID
- 155145
- Orphanet ID
- 1993
- Raras disease ID
- D01993
- UMLS CUI
- C1835087
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