Disease #06319 (SEDN (Spondyloepiphyseal dysplasia, Nishimura type), OMIM:618618)

Official abbreviation SEDN
Name Spondyloepiphyseal dysplasia, Nishimura type
OMIM ID 618618
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MIR140
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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