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- Piebaldism abstract "Piebaldism is a rare autosomal dominant disorder of melanocyte development. Common characteristics include a congenital white forelock, scattered normal pigmented and hypopigmented macules and a triangular shaped depigmented patch on the forehead.Although piebaldism may visually appear to be partial albinism, it is a fundamentally different condition. The vision problems associated with albinism are not usually present as eye pigmentation is normal. Piebaldism differs from albinism in that the affected cells maintain the ability to produce pigment but have that specific function turned off. In albinism the cells lack the ability to produce pigment altogether. It may be associated with KIT or SNAI2.".
- Piebaldism diseasesdb "29295".
- Piebaldism emedicineSubject "derm".
- Piebaldism emedicineTopic "689".
- Piebaldism icd10 "E70.3 (ILDS E70.350)".
- Piebaldism icd9 "709.09".
- Piebaldism meshId "D016116".
- Piebaldism omim "172800".
- Piebaldism wikiPageID "5070047".
- Piebaldism wikiPageRevisionID "592794921".
- Piebaldism diseasesdb "29295".
- Piebaldism emedicinesubj "derm".
- Piebaldism emedicinetopic "689".
- Piebaldism hasPhotoCollection Piebaldism.
- Piebaldism icd "709.09".
- Piebaldism icd "E70.3".
- Piebaldism meshid "D016116".
- Piebaldism name "Piebaldism".
- Piebaldism omim "172800".
- Piebaldism wordnet_type synset-disease-noun-1.
- Piebaldism subject Category:Amino_acid_metabolism_disorders.
- Piebaldism subject Category:Autosomal_dominant_disorders.
- Piebaldism subject Category:Disturbances_of_human_pigmentation.
- Piebaldism subject Category:Disturbances_of_pigmentation.
- Piebaldism type Abstraction100002137.
- Piebaldism type Act100030358.
- Piebaldism type Activity100407535.
- Piebaldism type AminoAcidMetabolismDisorders.
- Piebaldism type Attribute100024264.
- Piebaldism type AutosomalDominantDisease114162025.
- Piebaldism type AutosomalDominantDisorders.
- Piebaldism type Condition113920835.
- Piebaldism type Disease114070360.
- Piebaldism type Disorder114052403.
- Piebaldism type DisturbancesOfHumanPigmentation.
- Piebaldism type Event100029378.
- Piebaldism type GeneticDisease114151139.
- Piebaldism type IllHealth114052046.
- Piebaldism type Illness114061805.
- Piebaldism type PathologicalState114051917.
- Piebaldism type Perturbation107428450.
- Piebaldism type PhysicalCondition114034177.
- Piebaldism type PsychologicalFeature100023100.
- Piebaldism type State100024720.
- Piebaldism type YagoPermanentlyLocatedEntity.
- Piebaldism type Disease.
- Piebaldism type AilmentCondition.
- Piebaldism type Situation.
- Piebaldism comment "Piebaldism is a rare autosomal dominant disorder of melanocyte development. Common characteristics include a congenital white forelock, scattered normal pigmented and hypopigmented macules and a triangular shaped depigmented patch on the forehead.Although piebaldism may visually appear to be partial albinism, it is a fundamentally different condition. The vision problems associated with albinism are not usually present as eye pigmentation is normal.".
- Piebaldism label "Piebaldism".
- Piebaldism label "Piebaldismo".
- Piebaldism label "Piebaldismus".
- Piebaldism label "Piebaldyzm".
- Piebaldism label "Piébaldisme".
- Piebaldism sameAs Piebaldismus.
- Piebaldism sameAs Piebaldismo.
- Piebaldism sameAs Piébaldisme.
- Piebaldism sameAs Piebaldyzm.
- Piebaldism sameAs m.0d1bfl.
- Piebaldism sameAs Q1516083.
- Piebaldism sameAs Q1516083.
- Piebaldism sameAs 3586.
- Piebaldism sameAs 927.
- Piebaldism sameAs Piebaldism.
- Piebaldism wasDerivedFrom Piebaldism?oldid=592794921.
- Piebaldism isPrimaryTopicOf Piebaldism.
- Piebaldism name "Piebaldism".