Aqueductal stenosis
Symptom Information:
Symptom ID: | HPO:0002410 | ||||||||||||||
Synonyms: |
|
||||||||||||||
Quality: | |||||||||||||||
Cross references: |
|
||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||
Is a (Whole tree): |
HPO:
MedDRA: Nervous system disorders(MedDRA:10029205) Increased intracranial pressure and hydrocephalus(MedDRA:10021666) Hydrocephalic conditions(MedDRA:10020509) Aqueductal stenosis(HPO:0002410) |
||||||||||||||
Database Frequency: | 19 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
Alexander disease | (Orphanet:58) |
CHARGE syndrome | (Orphanet:138) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Craniomicromelic syndrome | (Orphanet:1524) |
Diabetic embryopathy | (Orphanet:1926) |
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY | (OMIM:600906) |
ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS | (OMIM:600907) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Growth delay - hydrocephaly - lung hypoplasia | (Orphanet:3035) |
Hydrocephalus with stenosis of aqueduct of Sylvius | (Orphanet:2182) |
L1 syndrome | (Orphanet:275543) |
Nager syndrome | (Orphanet:245) |
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion | (Orphanet:363700) |
Pfeiffer syndrome type 1 | (Orphanet:93258) |
Pfeiffer syndrome type 2 | (Orphanet:93259) |
Pfeiffer syndrome type 3 | (Orphanet:93260) |
VACTERL ASSOCIATION WITH HYDROCEPHALUS | (OMIM:276950) |
VACTERL with hydrocephalus | (Orphanet:3412) |