Complex hereditary spastic paraplegia
ORPHA:102013Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818Autosomal dominant complex spastic paraplegia
ORPHA:100979Autosomal recessive complex spastic paraplegia
ORPHA:100981Carney complex
ORPHA:1359Cloacal exstrophy
ORPHA:93929Femur-fibula-ulna complex
ORPHA:2019Shone complex
ORPHA:99063X-linked complex spastic paraplegia
ORPHA:98888Xeroderma pigmentosum-Cockayne syndrome complex
ORPHA:220295Xp21 deletion syndrome
ORPHA:261476