Disease #06863 (MRXSPM (?Paganini-Miozzo syndrome), OMIM:301025)

Official abbreviation MRXSPM
Name ?Paganini-Miozzo syndrome
OMIM ID 301025
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene HS6ST2
Associated tissues -
Disease features -
Remarks -

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