Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
CONGENITAL HYDROCEPHALUS	C0020256	CCDC88C	Causal	—	Disgenet
		PTCH1	Causal	—	Disgenet
		SMARCC1	Causal	—	Disgenet
		TRIM71	Causal	—	Disgenet
		IPO11	Unknown	—	Disgenet
		MPDZ	Unknown	—	Disgenet
		RANBP17	Unknown	—	Disgenet
		SGCD	Unknown	—	Disgenet
HYDROCEPHALUS WITH STENOSIS OF THE AQUEDUCT OF SYLVIUS	2182	L1CAM	Unknown	20301657	Orphanet
HYDROCEPHALUS, CONGENITAL COMMUNICATING, 1	MONDO:0032862	TRIM71	Causal	19098426 29216221 29434669 29983323 31371437 33077954	ClinVar GWAS catalog
HYDROCEPHALUS, CONGENITAL, 1	236600 C3887608	CCDC88C	Unknown	—	Disgenet HPO
		DOCK6	Unknown	—	Disgenet
		FSD1L	Unknown	—	Disgenet
HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES	C3554691 615219 OMIM:615219	ACADM	Unknown	—	Disgenet
		ANO6	Unknown	—	Disgenet
		MPDZ	Unknown	—	CTD Disgenet HPO
HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES	617967 C4747885 MONDO:0054794	WDR81	Causal	—	ClinVar Disgenet HPO
HYDROCEPHALUS, CONGENITAL, 4	618667 C5231454	TRIM71	Unknown	—	Disgenet HPO
HYDROCEPHALUS, CONGENITAL, 5, SUSCEPTIBILITY TO	MONDO:0859376	SMARCC1	Causal	29360170 29983323 33077954 37285932	ClinVar Disgenet
HYDROCEPHALUS, CONGENITAL, X-LINKED	307000	L1CAM	Unknown	—	HPO
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1	MONDO:0009360	CCDC88C	Causal	23042809	ClinVar GWAS catalog
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 2	MONDO:0014085	MPDZ	Causal	—	ClinVar GenCC
HYDROCEPHALUS, X-LINKED	MESH:C536078	L1CAM	Unknown	7920659 7920660	CTD
HYDROCEPHALUS, X-LINKED, WITH CONGENITAL IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION	C1844006	L1CAM	Causal	—	Disgenet

Congenital hydrocephalus