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Statements

Subject Item
dbr:Pai_syndrome
rdf:type
dbo:Disease wikidata:Q12136 owl:Thing
rdfs:label
Pai syndrome
rdfs:comment
Pai syndrome, also known as Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome, is a very rare genetic disorder which is characterized by nervous system, cutaneous, ocular, nasal and bucal anomalies with facial dysmorphisms.
dbp:name
Pai syndrome
foaf:depiction
n5:Cleftlipandpalate.jpg
dcterms:subject
dbc:Genetic_diseases_and_disorders
dbo:wikiPageID
70999089
dbo:wikiPageRevisionID
1117556487
dbo:wikiPageWikiLink
dbr:Short_stature dbr:Cleft_lip dbr:Genetic_disorder dbr:Bifid_uvula dbr:Palpebral_fissure dbr:Chromosome_Xq28 dbr:Chromosomal_translocation dbr:De_novo_mutation dbr:Corpus_callosum dbr:Intellectual_disabilities dbr:Chromosome_16 dbr:Frontal_bossing dbr:Skin_tags dbr:Subcutaneous_nodule dbr:Telecanthus dbr:Medical_genetics dbr:Encephalocele dbr:Coloboma dbr:Hypertelorism dbr:Genetic_mutation dbc:Genetic_diseases_and_disorders
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wikidata:Q47461585 n13:4PyXs
dbp:specialty
dbr:Medical_genetics
dbp:wikiPageUsesTemplate
dbt:Reflist dbt:Infobox_medical_condition dbt:Orphan
dbo:thumbnail
n5:Cleftlipandpalate.jpg?width=300
dbp:deaths
-
dbp:causes
dbr:Genetic_mutation
dbp:frequency
very rare, between 10-80 cases have been described in medical literature
dbp:synonyms
Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome
dbo:abstract
Pai syndrome, also known as Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome, is a very rare genetic disorder which is characterized by nervous system, cutaneous, ocular, nasal and bucal anomalies with facial dysmorphisms.
dbp:prevention
none
dbp:prognosis
Good
prov:wasDerivedFrom
wikipedia-en:Pai_syndrome?oldid=1117556487&ns=0
dbo:wikiPageLength
4162
dbo:alias
Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome
foaf:isPrimaryTopicOf
wikipedia-en:Pai_syndrome
Subject Item
wikipedia-en:Pai_syndrome
foaf:primaryTopic
dbr:Pai_syndrome