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- Tietz_syndrome abstract "Tietz syndrome, also called Tietz albinism-deafness syndrome or albinism and deafness of Tietz, is an autosomal dominant congenital disorder characterized by deafness and leucism. It is caused by a mutation in the microphthalmia-associated transcription factor (MITF) gene. Tietz syndrome was first described in 1923.".
- Tietz_syndrome diseasesdb "34108".
- Tietz_syndrome icd10 "E70.3(ILDS E70.358)".
- Tietz_syndrome omim "103500".
- Tietz_syndrome thumbnail Autosomal_dominant_-_en.svg?width=300.
- Tietz_syndrome wikiPageID "317453".
- Tietz_syndrome wikiPageRevisionID "593190076".
- Tietz_syndrome diseasesdb "34108".
- Tietz_syndrome hasPhotoCollection Tietz_syndrome.
- Tietz_syndrome icd "E70.3".
- Tietz_syndrome name "Tietz syndrome".
- Tietz_syndrome omim "103500".
- Tietz_syndrome wordnet_type synset-disease-noun-1.
- Tietz_syndrome subject Category:Autosomal_dominant_disorders.
- Tietz_syndrome subject Category:Congenital_disorders.
- Tietz_syndrome subject Category:Disturbances_of_human_pigmentation.
- Tietz_syndrome subject Category:Rare_diseases.
- Tietz_syndrome subject Category:Syndromes.
- Tietz_syndrome subject Category:Transcription_factor_deficiencies.
- Tietz_syndrome type Abnormality114501726.
- Tietz_syndrome type Abstraction100002137.
- Tietz_syndrome type Act100030358.
- Tietz_syndrome type Activity100407535.
- Tietz_syndrome type Anomaly114505821.
- Tietz_syndrome type Attribute100024264.
- Tietz_syndrome type AutosomalDominantDisease114162025.
- Tietz_syndrome type AutosomalDominantDisorders.
- Tietz_syndrome type BirthDefect114465048.
- Tietz_syndrome type Cognition100023271.
- Tietz_syndrome type Complex105870365.
- Tietz_syndrome type Concept105835747.
- Tietz_syndrome type Condition113920835.
- Tietz_syndrome type CongenitalDisorders.
- Tietz_syndrome type Content105809192.
- Tietz_syndrome type Defect114464005.
- Tietz_syndrome type Disease114070360.
- Tietz_syndrome type DisturbancesOfHumanPigmentation.
- Tietz_syndrome type Event100029378.
- Tietz_syndrome type GeneticDisease114151139.
- Tietz_syndrome type Idea105833840.
- Tietz_syndrome type IllHealth114052046.
- Tietz_syndrome type Illness114061805.
- Tietz_syndrome type Imperfection114462666.
- Tietz_syndrome type Lack114449405.
- Tietz_syndrome type Need114449126.
- Tietz_syndrome type PathologicalState114051917.
- Tietz_syndrome type Perturbation107428450.
- Tietz_syndrome type PhysicalCondition114034177.
- Tietz_syndrome type PsychologicalFeature100023100.
- Tietz_syndrome type State100024720.
- Tietz_syndrome type Syndrome105870790.
- Tietz_syndrome type Syndromes.
- Tietz_syndrome type TranscriptionFactorDeficiencies.
- Tietz_syndrome type Whole105869584.
- Tietz_syndrome type YagoPermanentlyLocatedEntity.
- Tietz_syndrome type Disease.
- Tietz_syndrome type AilmentCondition.
- Tietz_syndrome type Situation.
- Tietz_syndrome comment "Tietz syndrome, also called Tietz albinism-deafness syndrome or albinism and deafness of Tietz, is an autosomal dominant congenital disorder characterized by deafness and leucism. It is caused by a mutation in the microphthalmia-associated transcription factor (MITF) gene. Tietz syndrome was first described in 1923.".
- Tietz_syndrome label "Tietz syndrome".
- Tietz_syndrome label "Zespół Tietza".
- Tietz_syndrome sameAs Zespół_Tietza.
- Tietz_syndrome sameAs m.01v0f4.
- Tietz_syndrome sameAs Q7801152.
- Tietz_syndrome sameAs Q7801152.
- Tietz_syndrome sameAs 1136.
- Tietz_syndrome sameAs Tietz_syndrome.
- Tietz_syndrome wasDerivedFrom Tietz_syndrome?oldid=593190076.
- Tietz_syndrome depiction Autosomal_dominant_-_en.svg.
- Tietz_syndrome isPrimaryTopicOf Tietz_syndrome.
- Tietz_syndrome name "Tietz syndrome".