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- Cockayne_syndrome abstract "Cockayne syndrome (also called Weber-Cockayne syndrome, or Neill-Dingwall syndrome) is a rare autosomal recessive, congenital disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. Hearing loss and eye abnormalities (pigmentary retinopathy) are other common features, but problems with any or all of the internal organs are possible. It is associated with a group of disorders called leukodystrophies (conditions characterized by degradation of white matter). The underlying disorder is a defect in a DNA repair mechanism.It is named after English physician Edward Alfred Cockayne (1880–1956) and English dermatologist Frederick Parkes Weber (1863–1962). Neill-Dingwall syndrome was named after Mary M. Dingwall and Catherine A. Neill.".
- Cockayne_syndrome diseasesdb "2907".
- Cockayne_syndrome emedicineSubject "ped".
- Cockayne_syndrome emedicineTopic "424".
- Cockayne_syndrome icd10 "Q87.1 (ILDS Q87.110)".
- Cockayne_syndrome icd9 "759.8".
- Cockayne_syndrome meshId "D003057".
- Cockayne_syndrome omim "216400".
- Cockayne_syndrome thumbnail Autorecessive.svg?width=300.
- Cockayne_syndrome wikiPageExternalLink ghr.nlm.nih.gov.
- Cockayne_syndrome wikiPageExternalLink www.amyandfriends.org.
- Cockayne_syndrome wikiPageExternalLink main.
- Cockayne_syndrome wikiPageID "1493053".
- Cockayne_syndrome wikiPageRevisionID "594123043".
- Cockayne_syndrome caption "a child with cockayne syndrome".
- Cockayne_syndrome diseasesdb "2907".
- Cockayne_syndrome emedicinesubj "ped".
- Cockayne_syndrome emedicinetopic "424".
- Cockayne_syndrome hasPhotoCollection Cockayne_syndrome.
- Cockayne_syndrome icd "759.8".
- Cockayne_syndrome icd "Q87.1".
- Cockayne_syndrome meshid "D003057".
- Cockayne_syndrome name "Cockayne syndrome".
- Cockayne_syndrome omim "216400".
- Cockayne_syndrome wordnet_type synset-disease-noun-1.
- Cockayne_syndrome subject Category:Autosomal_recessive_disorders.
- Cockayne_syndrome subject Category:DNA_replication_and_repair-deficiency_disorders.
- Cockayne_syndrome subject Category:Genodermatoses.
- Cockayne_syndrome subject Category:Neurological_disorders.
- Cockayne_syndrome subject Category:Progeroid_syndromes.
- Cockayne_syndrome subject Category:Rare_diseases.
- Cockayne_syndrome subject Category:Syndromes.
- Cockayne_syndrome type Abstraction100002137.
- Cockayne_syndrome type Attribute100024264.
- Cockayne_syndrome type AutosomalRecessiveDisorders.
- Cockayne_syndrome type Cognition100023271.
- Cockayne_syndrome type Complex105870365.
- Cockayne_syndrome type Concept105835747.
- Cockayne_syndrome type Condition113920835.
- Cockayne_syndrome type Content105809192.
- Cockayne_syndrome type Disease114070360.
- Cockayne_syndrome type Disorder114052403.
- Cockayne_syndrome type Idea105833840.
- Cockayne_syndrome type IllHealth114052046.
- Cockayne_syndrome type Illness114061805.
- Cockayne_syndrome type NervousDisorder114084880.
- Cockayne_syndrome type NeurologicalDisorders.
- Cockayne_syndrome type PathologicalState114051917.
- Cockayne_syndrome type PhysicalCondition114034177.
- Cockayne_syndrome type PsychologicalFeature100023100.
- Cockayne_syndrome type State100024720.
- Cockayne_syndrome type Syndrome105870790.
- Cockayne_syndrome type Syndromes.
- Cockayne_syndrome type Whole105869584.
- Cockayne_syndrome type Disease.
- Cockayne_syndrome type AilmentCondition.
- Cockayne_syndrome type Situation.
- Cockayne_syndrome comment "Cockayne syndrome (also called Weber-Cockayne syndrome, or Neill-Dingwall syndrome) is a rare autosomal recessive, congenital disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. Hearing loss and eye abnormalities (pigmentary retinopathy) are other common features, but problems with any or all of the internal organs are possible.".
- Cockayne_syndrome label "Cockayne syndrome".
- Cockayne_syndrome label "Cockayne-Syndrom".
- Cockayne_syndrome label "Sindrome di Cockayne".
- Cockayne_syndrome label "Syndrome de Cockayne".
- Cockayne_syndrome label "Síndrome de Cockayne".
- Cockayne_syndrome label "Síndrome de Cockayne".
- Cockayne_syndrome label "Zespół Cockayne'a".
- Cockayne_syndrome label "متلازمة كوكاين".
- Cockayne_syndrome label "コケイン症候群".
- Cockayne_syndrome label "柯凱因氏症候群".
- Cockayne_syndrome sameAs Cockayne-Syndrom.
- Cockayne_syndrome sameAs Síndrome_de_Cockayne.
- Cockayne_syndrome sameAs Syndrome_de_Cockayne.
- Cockayne_syndrome sameAs Sindrome_di_Cockayne.
- Cockayne_syndrome sameAs コケイン症候群.
- Cockayne_syndrome sameAs Zespół_Cockayne'a.
- Cockayne_syndrome sameAs Síndrome_de_Cockayne.
- Cockayne_syndrome sameAs m.055nxc.
- Cockayne_syndrome sameAs Q914389.
- Cockayne_syndrome sameAs Q914389.
- Cockayne_syndrome sameAs 209.
- Cockayne_syndrome sameAs 247.
- Cockayne_syndrome sameAs Cockayne_syndrome.
- Cockayne_syndrome wasDerivedFrom Cockayne_syndrome?oldid=594123043.
- Cockayne_syndrome depiction Autorecessive.svg.
- Cockayne_syndrome isPrimaryTopicOf Cockayne_syndrome.
- Cockayne_syndrome name "Cockayne syndrome".
