About: Tyrosinemia type II

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Tyrosinemia type II is an autosomal recessive condition with onset between ages 2 and 4 years, when painful circumscribed calluses develop on the pressure points of the palm of the hand and sole of the foot.

Attributes	Values
rdf:type	Thing Fuchs' dystrophy yago:WikicatAminoAcidMetabolismDisorders yago:WikicatAutosomalRecessiveDisorders yago:WikicatMetabolicDisorders yago:WikicatPalmoplantarKeratodermas yago:Abstraction100002137 yago:Act100030358 yago:Attribute100024264 yago:Condition113920835 yago:Disease114070360 yago:Disorder114052403 yago:Event100029378 yago:IllHealth114052046 yago:Illness114061805 yago:Keratoderma114227906 yago:MetabolicDisorder114084502 yago:Mistake100070965 yago:Nonaccomplishment100066216 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatInbornErrorsOfMetabolism yago:YagoPermanentlyLocatedEntity disease yago:SkinDisease114219661 yago:State100024720
rdfs:label	Tirosinemia tipo 2 (es) Tyrosinemia type II (en)
rdfs:comment	La tirosinemia tipo II (también conocida como "tirosinemia Oculocutánea" y "síndrome de Richner-Hanhart" es una enfermedad de herencia autosómica recesiva, la cual se establece entre los 2 y 4 años de edad, cuando aparecen callosidades circunscritas que provocan un gran dolor en los puntos de presión de la palma y la planta del pie (es) Tyrosinemia type II is an autosomal recessive condition with onset between ages 2 and 4 years, when painful circumscribed calluses develop on the pressure points of the palm of the hand and sole of the foot. (en)
differentFrom	Hanhart syndrome
name	Tyrosinemia type II (en)
foaf:depiction
dcterms:subject	Autosomal recessive disorders Amino acid metabolism disorders Palmoplantar keratodermas
Wikipage page ID	21510326 (xsd:integer)
Wikipage revision ID	1098178722 (xsd:integer)
Link from a Wikipage to another Wikipage	Callus Pressure point American Academy of Dermatology Enzyme Autosomal recessive disorders Autosomal recessive Tyrosine Palmoplantar keratoderma Hand Amino acid metabolism disorders Tears Palmoplantar keratodermas Kidney Human eye Human skin Sole (foot) Heliophobia List of cutaneous conditions Tyrosine aminotransferase
sameAs	Tyrosinemia type II Tyrosinemia type II Tyrosinemia type II Tyrosinemia type II Tyrosinemia type II Tyrosinemia type II Tyrosinemia type II Tyrosinemia type II
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Distinguish dbt:EC_number dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Rp dbt:Amino_acid_metabolic_pathology dbt:Cutaneous-condition-stub
thumbnail	wiki-commons:Special:FilePath/L-tyrosine-skeletal.png?width=300
DiseasesDB	13486 (xsd:integer)
ICD	270.200000 (xsd:double) (en) E70.2 (en)
MeshID	D020176 (en)
OMIM	276600 (xsd:integer)
caption	Tyrosine
causes	Genetic (en)
field	American Academy of Dermatology
image size	180 (xsd:integer)
synonyms	Oculocutaneous tyrosinemia, Richner-Hanhart syndrome (en)
has abstract	La tirosinemia tipo II (también conocida como "tirosinemia Oculocutánea" y "síndrome de Richner-Hanhart" es una enfermedad de herencia autosómica recesiva, la cual se establece entre los 2 y 4 años de edad, cuando aparecen callosidades circunscritas que provocan un gran dolor en los puntos de presión de la palma y la planta del pie (es) Tyrosinemia type II is an autosomal recessive condition with onset between ages 2 and 4 years, when painful circumscribed calluses develop on the pressure points of the palm of the hand and sole of the foot. (en)
eMedicineSubj	ped (en)
eMedicineTopic	2339 (xsd:integer)
gold:hypernym	Condition
dbp:wordnet_type	http://www.w3.org/2006/03/wn/wn20/instances/synset-disease-noun-1
ICD9	270.2
eMedicine subject	ped (en)
eMedicine topic	2339 (en)
MeSH ID	D020176

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