Disease #00121 (LWD (LERI-WEILL DYSCHONDROSTEOSIS), OMIM:127300)

Official abbreviation LWD
Name LERI-WEILL DYSCHONDROSTEOSIS
OMIM ID 127300
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant, Y-linked
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SHOX
Associated tissues -
Disease features -
Remarks -

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