|
gptkbp:instanceOf
|
gptkb:disease
metabolic disorder
|
|
gptkbp:affects
|
gptkb:skin
gptkb:nervous_system
|
|
gptkbp:causedBy
|
abnormal function of heme biosynthesis enzymes
|
|
gptkbp:complication
|
hypertension
paralysis
chronic pain
liver damage
kidney damage
psychiatric disorders
|
|
gptkbp:diagnosedBy
|
blood test
urine test
stool test
|
|
gptkbp:firstDescribed
|
19th century
|
|
gptkbp:hasType
|
gptkb:acute_intermittent_porphyria
gptkb:acute_porphyria
gptkb:congenital_erythropoietic_porphyria
gptkb:cutaneous_porphyria
gptkb:erythropoietic_protoporphyria
gptkb:hereditary_coproporphyria
gptkb:porphyria_cutanea_tarda
gptkb:variegate_porphyria
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
Porphyria
|
|
gptkbp:inheritance
|
autosomal dominant
autosomal recessive
|
|
gptkbp:namedAfter
|
porphyrins
|
|
gptkbp:prevalence
|
rare
|
|
gptkbp:riskFactor
|
gptkb:beer
fasting
stress
genetic disorder
certain drugs
hormonal changes
|
|
gptkbp:symptom
|
vomiting
abdominal pain
muscle weakness
seizures
photosensitivity
psychiatric symptoms
blistering skin lesions
dark urine
|
|
gptkbp:treatment
|
gptkb:hemin
pain management
glucose
avoidance of triggers
|
|
gptkbp:bfsParent
|
gptkb:Porphyria's_Lover
|
|
gptkbp:bfsLayer
|
6
|