Communicating hydrocephalus
Symptom Information:
Symptom ID: | HPO:0001334 | |||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |