Disease #02785 (Spondyloepimetaphyseal dysplasia Matrilin-3 related, OMIM:608728)

Official abbreviation -
Name Spondyloepimetaphyseal dysplasia Matrilin-3 related
OMIM ID 608728
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 MATN3
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

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00230571 - - - - - - Arab, muslim - - - - Spondyloepimetaphyseal dysplasia Matrilin-3 related large consanguineous family MATN3 MATN3 2 1 LOVD
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