Communicating hydrocephalus

Symptom Information:

Symptom ID: HPO:0001334
Synonyms:
Acquired communicating hydrocephalus (disorder) [Orphanet:42480]
Communicating hydrocephalus (disorder) [Orphanet:42480]
Communicating Hydrocephalus [Orphanet:42480]
Non-obstructive hydrocephalus [Orphanet:42480]
Communicating hydrocephalus [OMIM:Communicating hydrocephalus]
Communicating hydrocephaly [Orphanet:42480]
Hydrocephaly communicative [Orphanet:42480]
Hydrocephalus [MedDRA:10020508]
Communicating hydrocephalus [MedDRA:10020508]
Hydrocephalus acquired [MedDRA:10020508]
Hydrocephalus NOS [MedDRA:10020508]
Hydrocephaly [MedDRA:10020508]
Hydrocephaly communicative [MedDRA:10020508]
Hydrocephaly obstructive [MedDRA:10020508]
Obstructive hydrocephalus [MedDRA:10020508]
Hydrocephalus (12%) [OMIM:Hydrocephalus (12%)]
Hydrocephalus (Dandy-Walker anomaly) [OMIM:Hydrocephalus (Dandy-Walker anomaly)]
Hydrocephalus (in 1 patient) [OMIM:Hydrocephalus (in 1 patient)]
Hydrocephalus (in 2 patients) [OMIM:Hydrocephalus (in 2 patients)]
Hydrocephalus (in some patients) [OMIM:Hydrocephalus (in some patients)]
Hydrocephalus (less common) [OMIM:Hydrocephalus (less common)]
Hydrocephalus (rare) [OMIM:Hydrocephalus (rare)]
Hydrocephalus (uncommon) [OMIM:Hydrocephalus (uncommon)]
Hydrocephalus (variable) [OMIM:Hydrocephalus (variable)]
Hydrocephalus, communicating [OMIM:Hydrocephalus, communicating]
Quality:
Cross references:
Orphanet:42480 "Communicating hydrocephaly" [Orphanet:42480]
OMIM: "Communicating hydrocephalus" [OMIM:Communicating hydrocephalus]
OMIM: "Hydrocephalus (12%)" [OMIM:Hydrocephalus (12%)]
OMIM: "Hydrocephalus (Dandy-Walker anomaly)" [OMIM:Hydrocephalus (Dandy-Walker anomaly)]
OMIM: "Hydrocephalus (in 1 patient)" [OMIM:Hydrocephalus (in 1 patient)]
OMIM: "Hydrocephalus (in 2 patients)" [OMIM:Hydrocephalus (in 2 patients)]
OMIM: "Hydrocephalus (in some patients)" [OMIM:Hydrocephalus (in some patients)]
OMIM: "Hydrocephalus (less common)" [OMIM:Hydrocephalus (less common)]
OMIM: "Hydrocephalus (rare)" [OMIM:Hydrocephalus (rare)]
OMIM: "Hydrocephalus (uncommon)" [OMIM:Hydrocephalus (uncommon)]
OMIM: "Hydrocephalus (variable)" [OMIM:Hydrocephalus (variable)]
OMIM: "Hydrocephalus, communicating" [OMIM:Hydrocephalus, communicating]
UMLS:C0009451 "Communicating Hydrocephalus" [Orphanet:42480]
UMLS:C0338593 "Non-obstructive hydrocephalus" [Orphanet:42480]
Is a (Direct Parents):
Orphanet Hydrocephalus
HPO         Hydrocephalus
MedDRA Hydrocephalic conditions
Is a (Whole tree): HPO:
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Increased intracranial pressure and hydrocephalus(MedDRA:10021666)
       Hydrocephalic conditions(MedDRA:10020509)
          Communicating hydrocephalus(HPO:0001334)
Database Frequency: 32 / 7739
Resource:

All diseases associated with this symptom:

ALG13-CDG (Orphanet:324422)
Aase-Smith syndrome (Orphanet:916)
Aniridia - renal agenesis - psychomotor retardation (Orphanet:1064)
Autosomal recessive cutis laxa type 2B (Orphanet:357064)
Beemer-Ertbruggen syndrome (Orphanet:1237)
Beta-mannosidosis (Orphanet:118)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
Chudley-McCullough syndrome (Orphanet:314597)
Cole-Carpenter syndrome (Orphanet:2050)
Dysmorphism - multiple structural anomalies (Orphanet:1780)
HEC syndrome (Orphanet:2119)
HOLOPROSENCEPHALY 5 (OMIM:609637)
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 2 (OMIM:615219)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hydrocephaly - low insertion umbilicus (Orphanet:2184)
ICF syndrome (Orphanet:2268)
Juvenile polyposis syndrome (Orphanet:2929)
Kozlowski-Brown-Hardwick syndrome (Orphanet:2352)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Proteus-like syndrome (Orphanet:2969)
Scheie syndrome (Orphanet:93474)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Thoracic dysplasia-hydrocephalus syndrome (Orphanet:1861)
X-linked centronuclear myopathy (Orphanet:596)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)