Disease #01390 (HPPA (hypophosphatasia, adult (odontohypophosphatasia)), OMIM:146300)

Official abbreviation HPPA
Name hypophosphatasia, adult (odontohypophosphatasia)
OMIM ID 146300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene ALPL
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00143197 - - - F - - - - - - - HPPA - ALPL ALPL 1 1 Dr. Alexandra Wey-Fabrizius
00143761 - - - F - - - - - - - HPPA - ALPL ALPL 2 1 Dr. Alexandra Wey-Fabrizius
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