Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHydrocephalus (D006849)
..Starting node
..expandHydrocephalus, Normal Pressure (D006850)

       Child Nodes:
........expandTremor, Hereditary Essential, And Idiopathic Normal Pressure Hydrocephalus (C567519)



 Sister Nodes: 
..expandAase Smith syndrome (C535332)
..expandAxenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities (C566234)
..expandBaker Vinters syndrome (C537899)
..expandBeemer Ertbruggen syndrome (C537668)
..expandBor-Duane hydrocephalus contiguous gene syndrome (C536574)
..expandClark-Baraitser syndrome (C536208)
..expandCole Carpenter syndrome (C535963)
..expandCystic Kidney Disease with Ventriculomegaly (C565657)
..expandDaentl Towsend Siegel syndrome (C535768)
..expandDaish Hardman Lamont syndrome (C535770)
..expandDandy-Walker Syndrome (D003616) Child13
..expandEdinburgh Malformation Syndrome (C563051)
..expandEnamel Hypoplasia, Cataracts, and Aqueductal Stenosis (C563430)
..expandGame Friedman Paradice syndrome (C535406)
..expandHydrocephalus With Cerebellar Agenesis (C564407)
..expandHydrocephalus, Autosomal Dominant (C563973)
..expandHydrocephalus, endocardial fibroelastosis, and cataracts (C535855)
..expandHydrocephalus, Normal Pressure (D006850) Child1
..expandHydrocephalus, Skeletal Anomalies, and Mental Disturbance (C563413)
..expandHydrocephalus, X-linked (C536078)
..expandHydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction (C564408)
..expandHydrolethalus syndrome (C536079)
..expandHydrolethalus Syndrome 1 (C565504)
..expandIris dysplasia hypertelorism deafness (C535537)
..expandKozlowski Brown Hardwick syndrome (C537506)
..expandMegalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome (C566381)
..expandOsteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (C563478)
..expandPalmer Pagon syndrome (C538107)
..expandRadius absent anogenital anomalies (C535281)
..expandSchwartz Cohen-Addad Lambert syndrome (C535835)
..expandThoracic Dysplasia-Hydrocephalus Syndrome (C564774)
..expandVACTERL Association With Hydrocephalus (C564751)
..expandVACTERL association with hydrocephaly, X-linked (C536520)
..expandVACTERL hydrocephaly (C536521)
..expandVater Association With Hydrocephalus (C564752)
..expandVentriculomegaly With Defects Of The Radius And Kidney (C566565)
..expandWaaler Aarskog syndrome (C536461)
..expandYim Ebbin syndrome (C536713)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5308
Name:Hydrocephalus, Normal Pressure
Definition:A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3)
Alternative IDs:OMIM:236690
ParentIDs:MESH:D006849
TreeNumbers:C10.228.140.602.559
Synonyms:Hakim's Syndrome |Hakims Syndrome |Hakim's Syndromes |Hakim Syndrome |Hakim Syndromes |Hydrocephalus, Normal-Pressure |Normal Pressure Hydrocephalus |NPH (Normal Pressure Hydrocephalus) |NPHs (Normal Pressure Hydrocephalus) |Syndrome, Hakim |Syndrome, Hakim's |Synd
Slim Mappings:Nervous system disease
Reference: MedGen: D006850
MeSH: D006850
OMIM: 236690;

Genes:
Phenotypes
1 HP:0000007Autosomal recessive inheritance
2 HP:0002607Bowel incontinence
3 HP:0000726Dementia
4 HP:0001288Gait disturbance
5 HP:0001263Global developmental delay
6 HP:0002343Normal pressure hydrocephalus
7 HP:0000020Urinary incontinence
Disease Causing ClinVar Variants