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psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive syndrome characterized by early-childhood onset of different combinations of intellectual disability, muscle weakness, camptocormia, oculomotor apraxia, and nephropathy.
Mondo Term and Equivalent IDs
MONDO:0044726:  psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome
Orphanet:505242: 
UMLS:CN353477: