Matches in DBpedia 2014 for { <http://dbpedia.org/resource/CAMFAK_syndrome> ?p ?o }
Showing triples 1 to 64 of
64
with 100 triples per page.
- CAMFAK_syndrome abstract "CAMFAK syndrome (or CAMAK syndrome) is an acronym used to describe a rare inherited neurologic disease, characterized by peripheral and central demyelination of nerves, similar to that seen in Cockayne syndrome. The name "CAMFAK" comes from the first letters of the characteristic findings of the disease: cataracts, microcephaly, failure to thrive, and kyphoscoliosis. The disease may occur with or without failure to thrive and arthrogryposis.".
- CAMFAK_syndrome diseasesdb "33725".
- CAMFAK_syndrome omim "212540".
- CAMFAK_syndrome thumbnail Autorecessive.jpg?width=300.
- CAMFAK_syndrome wikiPageExternalLink camfak_syndrome.html.
- CAMFAK_syndrome wikiPageExternalLink ABSTRACT?CRETRY=1&SRETRY=0.
- CAMFAK_syndrome wikiPageID "13406766".
- CAMFAK_syndrome wikiPageRevisionID "590849204".
- CAMFAK_syndrome diseasesdb "33725".
- CAMFAK_syndrome hasPhotoCollection CAMFAK_syndrome.
- CAMFAK_syndrome name "CAMFAK syndrome".
- CAMFAK_syndrome omim "212540".
- CAMFAK_syndrome wordnet_type synset-disease-noun-1.
- CAMFAK_syndrome subject Category:Autosomal_recessive_disorders.
- CAMFAK_syndrome subject Category:Congenital_disorders.
- CAMFAK_syndrome subject Category:Demyelinating_diseases_of_CNS.
- CAMFAK_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- CAMFAK_syndrome subject Category:Rare_diseases.
- CAMFAK_syndrome subject Category:Syndromes.
- CAMFAK_syndrome type Abnormality114501726.
- CAMFAK_syndrome type Abstraction100002137.
- CAMFAK_syndrome type Anomaly114505821.
- CAMFAK_syndrome type Attribute100024264.
- CAMFAK_syndrome type AutosomalRecessiveDisorders.
- CAMFAK_syndrome type BirthDefect114465048.
- CAMFAK_syndrome type Cognition100023271.
- CAMFAK_syndrome type Complex105870365.
- CAMFAK_syndrome type Concept105835747.
- CAMFAK_syndrome type Condition113920835.
- CAMFAK_syndrome type CongenitalDisorders.
- CAMFAK_syndrome type Content105809192.
- CAMFAK_syndrome type Defect114464005.
- CAMFAK_syndrome type Disease114070360.
- CAMFAK_syndrome type Disorder114052403.
- CAMFAK_syndrome type GeneticDisease114151139.
- CAMFAK_syndrome type GeneticDisordersWithOMIMButNoGene.
- CAMFAK_syndrome type Idea105833840.
- CAMFAK_syndrome type IllHealth114052046.
- CAMFAK_syndrome type Illness114061805.
- CAMFAK_syndrome type Imperfection114462666.
- CAMFAK_syndrome type NervousDisorder114084880.
- CAMFAK_syndrome type NeurologicalDisorders.
- CAMFAK_syndrome type PathologicalState114051917.
- CAMFAK_syndrome type PhysicalCondition114034177.
- CAMFAK_syndrome type PsychologicalFeature100023100.
- CAMFAK_syndrome type State100024720.
- CAMFAK_syndrome type Syndrome105870790.
- CAMFAK_syndrome type Syndromes.
- CAMFAK_syndrome type Whole105869584.
- CAMFAK_syndrome type Disease.
- CAMFAK_syndrome type AilmentCondition.
- CAMFAK_syndrome type Situation.
- CAMFAK_syndrome comment "CAMFAK syndrome (or CAMAK syndrome) is an acronym used to describe a rare inherited neurologic disease, characterized by peripheral and central demyelination of nerves, similar to that seen in Cockayne syndrome. The name "CAMFAK" comes from the first letters of the characteristic findings of the disease: cataracts, microcephaly, failure to thrive, and kyphoscoliosis. The disease may occur with or without failure to thrive and arthrogryposis.".
- CAMFAK_syndrome label "CAMFAK syndrome".
- CAMFAK_syndrome label "Zespół CAMFAK".
- CAMFAK_syndrome sameAs Zespół_CAMFAK.
- CAMFAK_syndrome sameAs m.03c4978.
- CAMFAK_syndrome sameAs Q5008650.
- CAMFAK_syndrome sameAs Q5008650.
- CAMFAK_syndrome sameAs CAMFAK_syndrome.
- CAMFAK_syndrome wasDerivedFrom CAMFAK_syndrome?oldid=590849204.
- CAMFAK_syndrome depiction Autorecessive.jpg.
- CAMFAK_syndrome isPrimaryTopicOf CAMFAK_syndrome.
- CAMFAK_syndrome name "CAMFAK syndrome".