Disease #05178 (MDST (dysplasia, metaphyseal, Spahr type (MDST)), OMIM:250400)

Official abbreviation MDST
Name dysplasia, metaphyseal, Spahr type (MDST)
OMIM ID 250400
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MMP13
Associated tissues -
Disease features -
Remarks -
Date created 2016-09-13 15:05:26 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00081039 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MDST Spahr type of metaphyseal dysplasia (OMIM:250400) MMP13 MMP13 1 1 Daniel Trujillano
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