Disease #04261 (SEDT (dysplasia, spondyloepiphyseal, tarda (SEDT)))

Official abbreviation SEDT
Name dysplasia, spondyloepiphyseal, tarda (SEDT)
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene COL2A1
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00038436 - PubMed: Nishimura 2005 - M ? - - - 0 - - SEDT - COL2A1 COL2A1 1 1 Isabelle Touitou
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