Odontohypophosphatasia
MONDO:0016607A particular form of hypophosphatasia (HPP) characterized by reduced activity of unfractionated serum alkaline phosphatase, premature exfoliation of primary and/or permanent teeth and/or severe dental caries, in the absence of skeletal system abnormalities. It can inherited via either autosomal dominant or autosomal recessive inheritance.
Also known as: HPPO, odonto-HPP
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Hypophosphatasia
(13)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
Developmental anomaly of metabolic origin
(0)
Disease by developmental or physiological process
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.