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- Van_der_Woude_syndrome abstract "Van Der Woude syndrome (VDWS) is a genetic disorder characterized by the combination of lower lip pits, cleft lip with or without cleft palate, and cleft palate alone (CP). The frequency of orofacial clefts ranges from 1:1000 to 1:500 births worldwide, and there are more than 400 syndromes that involve cleft lip with or without cleft palate. VWS is distinct from other clefting syndromes due to the combination of cleft lip and palate (CLP) and CP within the same family. Other features frequently associated with VWS include hypodontia in 10-81% of cases, narrow arched palate, congenital heart disease, heart murmur and cerebral abnormalities, syndactyly of the hands, polythelia, ankyloglossia, and adhesions between the upper and lower gum pads.The association between lower lip pits and cleft lip and/or palate was first described by Anne Van der Woude in 1954. The worldwide disease incidence ranges from 1:100,000 to 1:40,000.".
- Van_der_Woude_syndrome diseasesdb "31926".
- Van_der_Woude_syndrome emedicineSubject "ped".
- Van_der_Woude_syndrome emedicineTopic "2753".
- Van_der_Woude_syndrome icd10 "Q38.0".
- Van_der_Woude_syndrome omim "119300".
- Van_der_Woude_syndrome wikiPageID "2260123".
- Van_der_Woude_syndrome wikiPageRevisionID "598206047".
- Van_der_Woude_syndrome diseasesdb "31926".
- Van_der_Woude_syndrome emedicinesubj "ped".
- Van_der_Woude_syndrome emedicinetopic "2753".
- Van_der_Woude_syndrome hasPhotoCollection Van_der_Woude_syndrome.
- Van_der_Woude_syndrome icd "Q38.0".
- Van_der_Woude_syndrome name "Van der Woude syndrome".
- Van_der_Woude_syndrome omim "119300".
- Van_der_Woude_syndrome wordnet_type synset-disease-noun-1.
- Van_der_Woude_syndrome subject Category:Congenital_disorders.
- Van_der_Woude_syndrome subject Category:Genetic_disorders.
- Van_der_Woude_syndrome type Abnormality114501726.
- Van_der_Woude_syndrome type Abstraction100002137.
- Van_der_Woude_syndrome type Anomaly114505821.
- Van_der_Woude_syndrome type Attribute100024264.
- Van_der_Woude_syndrome type AutosomalDominantDisease114162025.
- Van_der_Woude_syndrome type AutosomalDominantDisorders.
- Van_der_Woude_syndrome type BirthDefect114465048.
- Van_der_Woude_syndrome type Cognition100023271.
- Van_der_Woude_syndrome type Complex105870365.
- Van_der_Woude_syndrome type Concept105835747.
- Van_der_Woude_syndrome type Condition113920835.
- Van_der_Woude_syndrome type CongenitalDisordersOfDigestiveSystem.
- Van_der_Woude_syndrome type CongenitalOralDisorders.
- Van_der_Woude_syndrome type Content105809192.
- Van_der_Woude_syndrome type Defect114464005.
- Van_der_Woude_syndrome type Disease114070360.
- Van_der_Woude_syndrome type Disorder114052403.
- Van_der_Woude_syndrome type GeneticDisease114151139.
- Van_der_Woude_syndrome type Idea105833840.
- Van_der_Woude_syndrome type IllHealth114052046.
- Van_der_Woude_syndrome type Illness114061805.
- Van_der_Woude_syndrome type Imperfection114462666.
- Van_der_Woude_syndrome type Lack114449405.
- Van_der_Woude_syndrome type Need114449126.
- Van_der_Woude_syndrome type PathologicalState114051917.
- Van_der_Woude_syndrome type PhysicalCondition114034177.
- Van_der_Woude_syndrome type PsychologicalFeature100023100.
- Van_der_Woude_syndrome type State100024720.
- Van_der_Woude_syndrome type Syndrome105870790.
- Van_der_Woude_syndrome type Syndromes.
- Van_der_Woude_syndrome type TranscriptionFactorDeficiencies.
- Van_der_Woude_syndrome type Whole105869584.
- Van_der_Woude_syndrome type Disease.
- Van_der_Woude_syndrome type AilmentCondition.
- Van_der_Woude_syndrome type Situation.
- Van_der_Woude_syndrome comment "Van Der Woude syndrome (VDWS) is a genetic disorder characterized by the combination of lower lip pits, cleft lip with or without cleft palate, and cleft palate alone (CP). The frequency of orofacial clefts ranges from 1:1000 to 1:500 births worldwide, and there are more than 400 syndromes that involve cleft lip with or without cleft palate. VWS is distinct from other clefting syndromes due to the combination of cleft lip and palate (CLP) and CP within the same family.".
- Van_der_Woude_syndrome label "Syndrome de Van der Woude".
- Van_der_Woude_syndrome label "Síndrome de Van der Woude".
- Van_der_Woude_syndrome label "Van der Woude syndrome".
- Van_der_Woude_syndrome label "Zespół van der Woude".
- Van_der_Woude_syndrome sameAs Síndrome_de_Van_der_Woude.
- Van_der_Woude_syndrome sameAs Syndrome_de_Van_der_Woude.
- Van_der_Woude_syndrome sameAs Zespół_van_der_Woude.
- Van_der_Woude_syndrome sameAs m.06zzyv.
- Van_der_Woude_syndrome sameAs Q2033532.
- Van_der_Woude_syndrome sameAs Q2033532.
- Van_der_Woude_syndrome sameAs 1256.
- Van_der_Woude_syndrome sameAs Van_der_Woude_syndrome.
- Van_der_Woude_syndrome wasDerivedFrom Van_der_Woude_syndrome?oldid=598206047.
- Van_der_Woude_syndrome isPrimaryTopicOf Van_der_Woude_syndrome.
- Van_der_Woude_syndrome name "Van der Woude syndrome".