Disease #01070 (SMAX3 (atrophy, muscular, spinal, distal, X-linked, type 3 (SMAX3)), OMIM:300489)

Official abbreviation SMAX3
Name atrophy, muscular, spinal, distal, X-linked, type 3 (SMAX3)
OMIM ID 300489
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ATP7A
Associated tissues -
Disease features -
Remarks -