Disease Term Disease ID Gene Symbol Classification References Source
Autosomal dominant spastic paraplegia type 9A 447753 ALDH18A1 Causal Pathogenic evidence from ClinVar - ClinVar
Autosomal dominant spastic paraplegia type 9B 447757 ALDH18A1 Causal Pathogenic evidence from ClinVar - ClinVar
Autosomal recessive spastic paraplegia type 9B 447760 ALDH18A1 Causal Pathogenic evidence from ClinVar - ClinVar
Spastic Paraplegia C0037772 ALDH18A1 Causal Pathogenic evidence from ClinVar - ClinVar
AP4B1 Causal Pathogenic evidence from ClinVar - ClinVar
AP4E1 Causal Pathogenic evidence from ClinVar - ClinVar
AP4M1 Causal Pathogenic evidence from ClinVar - ClinVar
AP4S1 Causal Pathogenic evidence from ClinVar 27444738 ClinVar
ATL1 Causal Pathogenic evidence from ClinVar - ClinVar
ATP13A2 Causal Pathogenic evidence from ClinVar - ClinVar
B4GALNT1 Causal Pathogenic evidence from ClinVar - ClinVar
CAPN1 Causal Pathogenic evidence from ClinVar - ClinVar
CYP2U1 Causal Pathogenic evidence from ClinVar - ClinVar
CYP7B1 Causal Pathogenic evidence from ClinVar 9802883, 18252231, 19439420, 19812052, 21214876, 21541746, 21623769, 23812641, 24117163, 24482476, 24519355 ClinVar
ERLIN2 Causal Pathogenic evidence from ClinVar - ClinVar
FA2H Causal Pathogenic evidence from ClinVar - ClinVar
GBA2 Causal Pathogenic evidence from ClinVar - ClinVar
SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) C1849115 ALDH18A1 Causal Pathogenic evidence from ClinVar - ClinVar
CYP7B1 Causal Pathogenic evidence from ClinVar 18252231, 19439420, 21214876, 21452256, 21541746, 21567895, 21623769, 22384504, 23812641, 24117163, 24658845, 26714052, 27217339, 29126212, 31337596 ClinVar
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) C1832669 ALDH18A1 Causal Pathogenic evidence from ClinVar 26026163, 26297558, 26320891, 29903433 ClinVar
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE C4225272 ALDH18A1 Causal Pathogenic evidence from ClinVar 26026163, 26297558, 29903433 ClinVar
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE C3279738 AP4B1 Causal Pathogenic evidence from ClinVar 21440262, 21620353, 22290197, 24700674, 24781758 ClinVar
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE C3151056 AP4E1 Causal Pathogenic evidence from ClinVar 20972249, 23472171 ClinVar
Spastic Paraplegia-50, Autosomal Recessive C2752008 AP4M1 Causal Pathogenic evidence from ClinVar 19559397, 29096665 ClinVar
SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE C3279743 AP4S1 Causal Pathogenic evidence from ClinVar 21620353, 25552650 ClinVar
Autosomal dominant spastic paraplegia type 3 100984 ATL1 Causal Pathogenic evidence from ClinVar - ClinVar
Spastic paraplegia 3, autosomal dominant C2931355 ATL1 Causal Pathogenic evidence from ClinVar 11685207, 12112092, 12499504, 12939451, 14607301, 14695538, 15184642, 15477516, 15517445, 15596607, 15742100, 16401858, 16533974, 16537571, 17321752, 17427918, 17502470, 17992088, 19459885, 19652243, 19768483, 20718791, 20816793, 20932283, 20947813, 21336785, 21368113, 22340599, 23079343, 23233086, 23483706, 23999326, 24417445, 24451228, 24473461, 24482476, 24604904, 25454648, 25637064, 25761634, 26671083, 29691679 ClinVar
Spastic Paraplegia, Hereditary C0037773 ATL1 Causal Pathogenic evidence from ClinVar 29691679 ClinVar
CYP2U1 Causal Pathogenic evidence from ClinVar 23176821 ClinVar
CYP7B1 Causal Pathogenic evidence from ClinVar 18252231, 28832565 ClinVar
ERLIN2 Causal Pathogenic evidence from ClinVar 23109145, 25977983, 28832565, 29528531 ClinVar
FA2H Causal Pathogenic evidence from ClinVar 27604308 ClinVar
GBA2 Causal Pathogenic evidence from ClinVar 28832565 ClinVar
Autosomal recessive spastic paraplegia type 78 513436 ATP13A2 Causal Pathogenic evidence from ClinVar - ClinVar
Complicated hereditary spastic paraplegia C0393556 ATP13A2 Causal Pathogenic evidence from ClinVar 27165006, 27217339, 28137957 ClinVar
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE C4310662 ATP13A2 Causal Pathogenic evidence from ClinVar 16964263, 21696388, 27165006, 27217339, 28137957, 29112700, 29859891 ClinVar
Autosomal recessive spastic paraplegia type 26 101006 B4GALNT1 Causal Pathogenic evidence from ClinVar - ClinVar
Autosomal recessive spastic paraplegia type 76 488594 CAPN1 Causal Pathogenic evidence from ClinVar - ClinVar
SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE C4310800 CAPN1 Causal Pathogenic evidence from ClinVar 27153400, 28566166 ClinVar
Autosomal recessive spastic paraplegia type 56 320411 CYP2U1 Causal Pathogenic evidence from ClinVar - ClinVar
SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE C3539507 CYP2U1 Causal Pathogenic evidence from ClinVar 23176821, 24337409 ClinVar
Autosomal Recessive Hereditary Spastic Paraplegia C0751603 CYP7B1 Causal Pathogenic evidence from ClinVar 18252231 ClinVar
Autosomal recessive spastic paraplegia type 5A 100986 CYP7B1 Causal Pathogenic evidence from ClinVar - ClinVar
Hereditary Autosomal Dominant Spastic Paraplegia C0751602 CYP7B1 Causal Pathogenic evidence from ClinVar 18252231 ClinVar
Hereditary X-Linked Recessive Spastic Paraplegia C0751604 CYP7B1 Causal Pathogenic evidence from ClinVar 18252231 ClinVar
Spastic paraplegia type 5A, recessive C2931356 CYP7B1 Causal Pathogenic evidence from ClinVar 19812052 ClinVar
Autosomal recessive spastic paraplegia type 18 209951 ERLIN2 Causal Pathogenic evidence from ClinVar - ClinVar
Autosomal recessive spastic paraplegia type 35 171629 FA2H Causal Pathogenic evidence from ClinVar - ClinVar
Autosomal recessive spastic paraplegia type 46 320391 GBA2 Causal Pathogenic evidence from ClinVar - ClinVar
SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE C2828721 GBA2 Causal Pathogenic evidence from ClinVar 23332916, 23332917, 24252062, 26220345, 28052128, 30308956 ClinVar