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- Adermatoglyphia abstract "Adermatoglyphia is a rare medical condition which causes a person to have no fingerprints. There are only four known extended families worldwide which are affected by this condition.Recently, the description of a case of a person from Switzerland lacking fingerprints as an isolated finding was published. The phenotype was mapped to chromosome 4q22. In the splice-site of a 3' exon of the gene for SMARCAD1-helicase, a point mutation was detected. It results in a shortened form of the skin-specific protein. The heterozygous mode of mutation suggests an autosomal dominant mode of inheritance.Other conditions can cause a lack of fingerprints, but unlike them, adermatoglyphia has no other side effects. Mutations in helicases are in involved in other rare genetic diseases, for instance Werner syndrome.".
- Adermatoglyphia omim "136000".
- Adermatoglyphia wikiPageID "32684937".
- Adermatoglyphia wikiPageRevisionID "592010239".
- Adermatoglyphia hasPhotoCollection Adermatoglyphia.
- Adermatoglyphia name "Adermatoglyphia".
- Adermatoglyphia omim "136000".
- Adermatoglyphia subject Category:Autosomal_dominant_disorders.
- Adermatoglyphia subject Category:Cutaneous_congenital_anomalies.
- Adermatoglyphia subject Category:Rare_diseases.
- Adermatoglyphia type Abnormality114501726.
- Adermatoglyphia type Abstraction100002137.
- Adermatoglyphia type Anomaly114505821.
- Adermatoglyphia type Attribute100024264.
- Adermatoglyphia type AutosomalDominantDisease114162025.
- Adermatoglyphia type AutosomalDominantDisorders.
- Adermatoglyphia type BirthDefect114465048.
- Adermatoglyphia type Condition113920835.
- Adermatoglyphia type CutaneousCongenitalAnomalies.
- Adermatoglyphia type Defect114464005.
- Adermatoglyphia type Disease114070360.
- Adermatoglyphia type GeneticDisease114151139.
- Adermatoglyphia type IllHealth114052046.
- Adermatoglyphia type Illness114061805.
- Adermatoglyphia type Imperfection114462666.
- Adermatoglyphia type PathologicalState114051917.
- Adermatoglyphia type PhysicalCondition114034177.
- Adermatoglyphia type State100024720.
- Adermatoglyphia type Disease.
- Adermatoglyphia type Situation.
- Adermatoglyphia comment "Adermatoglyphia is a rare medical condition which causes a person to have no fingerprints. There are only four known extended families worldwide which are affected by this condition.Recently, the description of a case of a person from Switzerland lacking fingerprints as an isolated finding was published. The phenotype was mapped to chromosome 4q22. In the splice-site of a 3' exon of the gene for SMARCAD1-helicase, a point mutation was detected.".
- Adermatoglyphia label "Adermatoglifia".
- Adermatoglyphia label "Adermatoglifia".
- Adermatoglyphia label "Adermatoglyphia".
- Adermatoglyphia label "Adermatoglyphie".
- Adermatoglyphia sameAs Adermatoglyphie.
- Adermatoglyphia sameAs Αδερματογλυφία.
- Adermatoglyphia sameAs Adermatoglifia.
- Adermatoglyphia sameAs Adermatoglifia.
- Adermatoglyphia sameAs Adermatoglifia.
- Adermatoglyphia sameAs m.0h3sypv.
- Adermatoglyphia sameAs Q356410.
- Adermatoglyphia sameAs Q356410.
- Adermatoglyphia sameAs Adermatoglyphia.
- Adermatoglyphia wasDerivedFrom Adermatoglyphia?oldid=592010239.
- Adermatoglyphia isPrimaryTopicOf Adermatoglyphia.
- Adermatoglyphia name "Adermatoglyphia".