Disease #00039 (XBSN (X-Linked Bulbo-Spinal Atrophy), OMIM:313200)

Official abbreviation XBSN
Name X-Linked Bulbo-Spinal Atrophy
OMIM ID 313200
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 0 genes -
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Disease features -
Remarks -

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