Disease #00330 (MANDP2 (anadysplasia, metaphyseal, type 2 (MANDP2)), OMIM:613073)

Official abbreviation MANDP2
Name anadysplasia, metaphyseal, type 2 (MANDP2)
OMIM ID 613073
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MMP9
Associated tissues -
Disease features -
Remarks -
Date created 2014-02-20 17:41:08 +01:00 (CET)
Date last edited 2021-06-21 14:56:07 +02:00 (CEST)


Individuals

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00376164 - - Case report currently under resubmission, Eur J Med Genet M yes Spain - - - - - MANDP2 scoliosis (HP:0002650), metaphyseal fraying (HP:0003025), genu valgum (HP:0002857) - MMP9 1 1 Karen E. Heath
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