Witteveen-Kolk syndrome
ORPHA:500163X-linked intellectual disability-ataxia-apraxia syndrome
ORPHA:85338X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome
ORPHA:480907← PrevPage 2 of 2
Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
Witteveen-Kolk syndrome
ORPHA:500163X-linked intellectual disability-ataxia-apraxia syndrome
ORPHA:85338X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome
ORPHA:480907