Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
PEROXISOME BIOGENESIS DISORDER	MONDO:0019234PS214100	PEX1	Causal	11389485 12717447 22871920 23247051 24503136 26387595 9398847	CTD ClinGen
		PEX10	Causal	10212151 10562279 10862081 17041890 19127411 19933170 20695019 9683594 9700193	ClinGen GWAS catalog
		PEX11B	Causal	12024045 12096124 21669930 22581968 24234511 28129423 31724321	ClinGen GWAS catalog
		PEX12	Causal	10837480 14571262 26319495 9090384 9354782 9632816 9792857	ClinGen ClinVar Orphanet
		PEX13	Causal	10332040 12096124 12897163 17041890 19449432 21031596 21669930	ClinGen GWAS catalog
		PEX16	Causal	11890679 12096124 20647552 20681997 21031596 21826223 24091540 25002403 26644994 30094183 9837814	ClinGen ClinVar GWAS catalog
		PEX19	Causal	10051604 12096124 20683989 21031596 21669930 22871920 28526747 30561787 36931687	ClinGen GWAS catalog
		PEX2	Causal	10891359 11478384 14630978 1546315 19687296 19933170 21392394 22500805 26833788 9452066	ClinGen Disgenet
		PEX26	Causal	12717447 12851857 15542397 15858711 17336976 28823628 30446579	ClinGen GWAS catalog
		PEX3	Causal	10958759 12096124 20033294 21031596 21677750 21826223 22871920 23245813 27557811 28673549	ClinGen Disgenet
		PEX5	Causal	10562279 11583975 18712838 26220973 27290639 7719337 9288097	ClinGen Disgenet
		PEX6	Causal	12717447 17041890 22871920 22894767 26387595 8670792	ClinGen ClinVar GWAS catalog
		PEX7	Causal	10083738 12325024 12915479 20060764 25538232 25800479 26450166 26587300 28742517 9090381	ClinGen Disgenet
		PEX14	Unknown	15146459 21686775 22871920 26627464 30224891 9094717	CTD ClinGen
PEROXISOME BIOGENESIS DISORDER 10A	614882 C3553999 MONDO:0013948 OMIM:614882	PEX3	Unknown	—	CTD ClinVar Disgenet GenCC HPO
PEROXISOME BIOGENESIS DISORDER 10B	617370 C4479254 MONDO:0054549 OMIM:617370	PEX3	Causal	27557811	CTD ClinVar Disgenet GWAS catalog HPO
PEROXISOME BIOGENESIS DISORDER 11A	614883 C3554000 MONDO:0013949 OMIM:614883	PEX13	Unknown	—	CTD ClinVar Disgenet GenCC HPO
PEROXISOME BIOGENESIS DISORDER 11A	614883 C3554000 MONDO:0013949 OMIM:614883	PUS10	Unknown	—	Disgenet
PEROXISOME BIOGENESIS DISORDER 11B	614885 C3554001 MONDO:0013950 OMIM:614885	PEX13	Causal	—	CTD ClinVar Disgenet GenCC HPO
PEROXISOME BIOGENESIS DISORDER 11B	614885 C3554001 MONDO:0013950 OMIM:614885	PUS10	Unknown	—	Disgenet
PEROXISOME BIOGENESIS DISORDER 12A	614886 C3554002 MONDO:0013951 OMIM:614886	PEX19	Unknown	—	CTD ClinVar Disgenet GenCC HPO
PEROXISOME BIOGENESIS DISORDER 13A	614887 C3554004 MONDO:0013952 OMIM:614887	PEX14	Unknown	—	CTD ClinVar Disgenet GenCC HPO
PEROXISOME BIOGENESIS DISORDER 14B	614920 C3554055 MONDO:0013967 OMIM:614920	PEX11B	Causal	28129423 22581968	CTD ClinVar Disgenet GWAS catalog HPO
PEROXISOME BIOGENESIS DISORDER 1A	C4721541 214100 MONDO:0008953	GATAD1	Unknown	—	Disgenet
		PAF1	Unknown	—	Disgenet
		PEX1	Unknown	—	ClinVar Disgenet GenCC HPO
		PEX10	Unknown	—	Disgenet
		PEX12	Unknown	—	Disgenet
		PEX13	Unknown	—	Disgenet
		PEX14	Unknown	—	Disgenet
		PEX16	Unknown	—	Disgenet
		PEX19	Unknown	—	Disgenet
		PEX2	Unknown	—	Disgenet
		PEX26	Unknown	—	Disgenet
		PEX3	Unknown	—	Disgenet
		PEX5	Unknown	—	Disgenet
		PEX6	Unknown	—	Disgenet
		PUS10	Unknown	—	Disgenet
		RER1	Unknown	—	Disgenet
		SAMD4B	Unknown	—	Disgenet
PEROXISOME BIOGENESIS DISORDER 1B	601539 MONDO:0011101	PEX1	Causal	16086329 16141001 20301621 21031596 26387595 31831025 9398847	ClinVar Disgenet HPO
PEROXISOME BIOGENESIS DISORDER 2A	C3550273 214110 MONDO:0008954 OMIM:214110	PEX5	Unknown	7719337	Disgenet
PEROXISOME BIOGENESIS DISORDER 2B	202370 C3550234 MONDO:0008736 OMIM:202370	PEX5	Causal	26220973	CTD ClinVar Disgenet GWAS catalog HPO
		PEX6	Causal	—	Disgenet
		ABCD1	Unknown	—	Disgenet
PEROXISOME BIOGENESIS DISORDER 3A	614859 MONDO:0013927 OMIM:614859 C3553929	PEX12	Unknown	—	CTD ClinVar GenCC HPO
PEROXISOME BIOGENESIS DISORDER 3B	266510 C3550693	PEX12	Unknown	—	Disgenet HPO
PEROXISOME BIOGENESIS DISORDER 4A	C3553936	PEX6	Unknown	—	Disgenet

Peroxisome biogenesis disorder