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Statements

Subject Item
dbr:Singleton_Merten_syndrome
rdf:type
yago:PhysicalCondition114034177 yago:WikicatGeneticDisordersWithNoOMIM dbo:Disease yago:WikicatAutosomalDominantDisorders wikidata:Q12136 yago:GeneticDisease114151139 yago:PathologicalState114051917 yago:State100024720 yago:AutosomalDominantDisease114162025 yago:Disease114070360 yago:Abstraction100002137 yago:Condition113920835 yago:Illness114061805 owl:Thing yago:IllHealth114052046 yago:Attribute100024264
rdfs:label
Singleton Merten syndrome
rdfs:comment
Singleton Merten syndrome is an autosomal dominant genetic disorder with variable expression with an onset of symptoms during childhood.
foaf:name
Singleton Merten syndrome
dbp:name
Singleton Merten syndrome
foaf:depiction
n19:Autosomal_dominant_-_en.svg
dcterms:subject
dbc:Genetic_disorders_with_no_OMIM dbc:Autosomal_dominant_disorders dbc:Rare_syndromes
dbo:wikiPageID
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dbo:wikiPageWikiLink
dbr:Skin dbr:Phalanx_bone dbr:IFIH1 dbr:Soft_tissue dbr:Skeleton dbr:Psoriasis dbr:Demineralization_(physiology) dbr:Body_of_radius dbr:Expressivity_(genetics) dbr:Coxa_valga dbr:Autosomal dbr:Calcification dbr:DDX58 dbr:Aorta dbr:Glaucoma dbr:Radius_(bone) dbr:Hypoplasia dbr:Alkaline_phosphatase dbr:Club_foot dbr:Deformity dbr:Ulna dbr:Anatomical_terms_of_location dbr:Genetic_disorder dbr:Femur_head dbc:Genetic_disorders_with_no_OMIM dbr:Patient dbr:Cardiomegaly dbr:Aortic_valve dbr:Heart_block dbr:Mitral_valve dbc:Autosomal_dominant_disorders dbr:Dentition dbr:Foot dbr:Chronic_(medicine) dbr:Acetabular_fossa dbr:Childhood dbr:Muscle_weakness dbr:Fever_of_unknown_origin dbr:Developmental_biology dbr:Medical_history dbr:Edward_B._Singleton dbr:Metacarpus dbr:Radiology dbr:Symptom dbr:Subluxation dbr:Epiphysis dbr:Calcium dbr:Photosensitivity_in_humans dbr:Lesion dbr:Phosphorus dbr:Medullary_cavity dbc:Rare_syndromes
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dbo:thumbnail
n19:Autosomal_dominant_-_en.svg?width=300
dbp:icd
Q78.8
dbp:omim
182250
dbp:orphanet
85191
dbp:caption
Singleton Merten syndrome is inherited in an autosomal dominant manner.
dbp:synonyms
Singleton-Merten dysplasia
dbo:abstract
Singleton Merten syndrome is an autosomal dominant genetic disorder with variable expression with an onset of symptoms during childhood.
gold:hypernym
dbr:Autosomal
prov:wasDerivedFrom
wikipedia-en:Singleton_Merten_syndrome?oldid=1084540565&ns=0
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