Hydrocephalus

Symptom Information:

Symptom ID: HPO:0000238
Synonyms:
Hydrocephaly [HPO:0000238]
Nonsyndromal hydrocephalus [HPO:0000238]
Hydrocephalus (disorder) [Orphanet:42450]
Hydrocephalus [Orphanet:42450]
Hydrocephalus [OMIM:Hydrocephalus]
Hydrocephaly [OMIM:Hydrocephaly]
Hydrocephaly [Orphanet:42450]
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:42450 "Hydrocephaly" [Orphanet:42450]
OMIM: "Hydrocephalus" [OMIM:Hydrocephalus]
OMIM: "Hydrocephaly" [OMIM:Hydrocephaly]
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:C0020255 "Hydrocephalus" [HPO:0000238]
UMLS:C0020255 "Hydrocephalus" [Orphanet:42450]
Is a (Direct Parents):
HPO         Abnormality of the cerebral ventricles
Orphanet Structural anomalies of the nervous system
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)
          Hydrocephalus(HPO:0000238)
Database Frequency: 278 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
1q21.1 microdeletion syndrome (Orphanet:250989)
1q21.1 microduplication syndrome (Orphanet:250994)
1q44 microdeletion syndrome (Orphanet:238769)
3C syndrome (Orphanet:7)
6p22 microdeletion syndrome (Orphanet:251046)
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
AICARDI-GOUTIERES SYNDROME 4 (OMIM:610333)
ALG13-CDG (Orphanet:324422)
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM (OMIM:104350)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
Aase-Smith syndrome (Orphanet:916)
Acalvaria (Orphanet:945)
Achondroplasia (Orphanet:15)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Acroosteolysis, dominant type (Orphanet:955)
Adams-Oliver syndrome (Orphanet:974)
Albers-Schönberg osteopetrosis (Orphanet:53)
Alexander disease (Orphanet:58)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Alpha-mannosidosis (Orphanet:61)
Amelo-cerebro-hypohidrotic syndrome (Orphanet:1946)
Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Antley-Bixler syndrome (Orphanet:83)
Apert syndrome (Orphanet:87)
Arachnoiditis (Orphanet:137817)
Arnold-Chiari malformation type II (Orphanet:1136)
Atypical teratoid tumor (Orphanet:99966)
Autosomal recessive cutis laxa type 2B (Orphanet:357064)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
B4GALT1-CDG (Orphanet:79332)
BRESEK syndrome (Orphanet:85284)
Baller-Gerold syndrome (Orphanet:1225)
Beemer-Ertbruggen syndrome (Orphanet:1237)
Biemond syndrome type 2 (Orphanet:141333)
Brachydactyly - nystagmus - cerebellar ataxia (Orphanet:1246)
CAMPOMELIC DYSPLASIA (OMIM:114290)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME (OMIM:613603)
CHROMOSOME 8q12.1-q21.2 DELETION SYNDROME (OMIM:600257)
COLE-CARPENTER SYNDROME 2 (OMIM:616294)
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME (OMIM:614195)
Campomelic dysplasia (Orphanet:140)
Cantrell pentalogy (Orphanet:1335)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Caudal appendage - deafness (Orphanet:1123)
Cerebellum agenesis - hydrocephaly (Orphanet:1397)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Chudley-McCullough syndrome (Orphanet:314597)
Cloacal exstrophy (Orphanet:93929)
Cobblestone lissencephaly without muscular or ocular involvement (Orphanet:352682)
Cole-Carpenter syndrome (Orphanet:2050)
Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome (Orphanet:363741)
Congenital hydrocephalus (Orphanet:2185)
Congenital toxoplasmosis (Orphanet:858)
Costello syndrome (Orphanet:3071)
Craniofacial dyssynostosis (Orphanet:1516)
Craniosynostosis - Dandy-Walker malformation - hydrocephalus (Orphanet:1538)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Craniotelencephalic dysplasia (Orphanet:1528)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cutis laxa (Orphanet:209)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Deafness - onychodystrophy (Orphanet:3231)
Desmosterolosis (Orphanet:35107)
Diabetic embryopathy (Orphanet:1926)
Diencephalic syndrome (Orphanet:1672)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal 7q11.23 microduplication syndrome (Orphanet:261102)
Dubowitz syndrome (Orphanet:235)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
EDINBURGH MALFORMATION SYNDROME (OMIM:129850)
EVC2 GENE (OMIM:607261)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Edinburgh malformation syndrome (Orphanet:1895)
Embryofetopathy due to oral anticoagulant therapy (Orphanet:1914)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
Exstrophy-epispadias complex (Orphanet:322)
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS (OMIM:227255)
FANCONI ANEMIA, COMPLEMENTATION GROUP L (OMIM:614083)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Familial lambdoid synostosis (Orphanet:3267)
Fanconi anemia (Orphanet:84)
Fetal akinesia deformation sequence (Orphanet:994)
Focal dermal hypoplasia (Orphanet:2092)
Fowler syndrome (Orphanet:221126)
Fraser syndrome (Orphanet:2052)
Free sialic acid storage disease, infantile form (Orphanet:309324)
Fried syndrome (Orphanet:85335)
Frontal encephalocele (Orphanet:1931)
Frontonasal dysplasia (Orphanet:250)
Gaucher disease (Orphanet:355)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Gaucher disease type 3 (Orphanet:77261)
Genito-palato-cardiac syndrome (Orphanet:2075)
Goldenhar syndrome (Orphanet:374)
Gorlin syndrome (Orphanet:377)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Griscelli disease (Orphanet:381)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
Gómez-López-Hernández syndrome (Orphanet:1532)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HOLOPROSENCEPHALY 5 (OMIM:609637)
HOLOPROSENCEPHALY 9 (OMIM:610829)
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1 (OMIM:236600)
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 2 (OMIM:615219)
HYDROLETHALUS SYNDROME 2 (OMIM:614120)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Hb Bart's hydrops fetalis (Orphanet:163596)
Histiocytoid cardiomyopathy (Orphanet:137675)
Holoprosencephaly (Orphanet:2162)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hurler syndrome (Orphanet:93473)
Hydatidosis (Orphanet:400)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hydrocephalus - obesity - hypogonadism (Orphanet:2183)
Hydrocephalus with stenosis of aqueduct of Sylvius (Orphanet:2182)
Hydrocephaly - tall stature - joint laxity (Orphanet:2181)
Hydrolethalus (Orphanet:2189)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Hypoplasminogenemia (Orphanet:722)
Infantile osteopetrosis with neuroaxonal dysplasia (Orphanet:85179)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures (Orphanet:1568)
Intellectual deficit, X-linked, Kroes type (Orphanet:163961)
Isolated Dandy-Walker malformation (Orphanet:217)
Isolated cloverleaf skull syndrome (Orphanet:2343)
Isolated spina bifida (Orphanet:823)
Isotretinoin-like syndrome (Orphanet:2306)
Jacobsen syndrome (Orphanet:2308)
Joubert syndrome (Orphanet:475)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome 2 (OMIM:608091)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with ocular defect (Orphanet:220493)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Joubert syndrome with renal defect (Orphanet:220497)
KLEEBLATTSCHAEDEL (OMIM:148800)
KRABBE DISEASE (OMIM:245200)
Kabuki syndrome (Orphanet:2322)
Knobloch syndrome (Orphanet:1571)
Krabbe disease (Orphanet:487)
L1 syndrome (Orphanet:275543)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Large congenital melanocytic nevus (Orphanet:626)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Laurin-Sandrow syndrome (Orphanet:2378)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal omphalocele-cleft palate syndrome (Orphanet:2736)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lethal polymalformative syndrome, Boissel type (Orphanet:210144)
Lhermitte-Duclos disease (Orphanet:65285)
Limb body wall complex (Orphanet:2369)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
Lymphangioleiomyomatosis (Orphanet:538)
MASA syndrome (Orphanet:2466)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2 (OMIM:615937)
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 (OMIM:615938)
MICROPHTHALMIA, SYNDROMIC 7 (OMIM:309801)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 11 (OMIM:615181)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 (OMIM:615249)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 13 (OMIM:615287)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 (OMIM:613150)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 (OMIM:253800)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 (OMIM:613153)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6 (OMIM:613154)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 8 (OMIM:614830)
Macrocephaly - short stature - paraplegia (Orphanet:2427)
Marden-Walker syndrome (Orphanet:2461)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 3 (OMIM:607361)
Meckel syndrome, type 4 (OMIM:611134)
Meckel syndrome, type 6 (OMIM:612284)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Metatropic dysplasia (Orphanet:2635)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Microphthalmia with limb anomalies (Orphanet:1106)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Muenke syndrome (Orphanet:53271)
Multiple sulfatase deficiency (Orphanet:585)
Muscle-eye-brain disease (Orphanet:588)
Mycophenolate mofetil embryopathy (Orphanet:268249)
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO (OMIM:182940)
Nager syndrome (Orphanet:245)
Nasu-Hakola disease (Orphanet:2770)
Nephronophthisis 18 (OMIM:615862)
Neural tube closure defect (Orphanet:268357)
Neurocutaneous melanocytosis (Orphanet:2481)
Neurofibromatosis type 1 (Orphanet:636)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION (OMIM:166990)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 (OMIM:259700)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5 (OMIM:259720)
Oculocerebral hypopigmentation syndrome, Preus type (Orphanet:2720)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Osteocraniostenosis (Orphanet:2763)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Oxoglutaricaciduria (Orphanet:31)
PEHO syndrome (Orphanet:2836)
PORENCEPHALY 1 (OMIM:175780)
Papilloma of choroid plexus (Orphanet:2807)
Pelviscapular dysplasia (Orphanet:93333)
Peters-plus syndrome (Orphanet:709)
Pfeiffer syndrome (Orphanet:710)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Porencephaly (Orphanet:2940)
Port-wine nevi - mega cisterna magna - hydrocephalus (Orphanet:2703)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Pycnodysostosis (Orphanet:763)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
ROBERTS SYNDROME (OMIM:268300)
Radius absent - anogenital anomalies (Orphanet:3016)
Rhombencephalosynapsis (Orphanet:59315)
Roberts syndrome (Orphanet:3103)
Robinow-like syndrome (Orphanet:3105)
Scheie syndrome (Orphanet:93474)
Severe achondroplasia - developmental delay - acanthosis nigricans (Orphanet:85165)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Steinert myotonic dystrophy (Orphanet:273)
Sturge-Weber syndrome (Orphanet:3205)
TEMPLE SYNDROME (OMIM:616222)
TENORIO SYNDROME (OMIM:616260)
Tetraamelia - multiple malformations (Orphanet:3301)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)
Triploidy (Orphanet:3376)
Trisomy 17p (Orphanet:261290)
Trisomy 1q (Orphanet:261344)
VACTERL ASSOCIATION WITH HYDROCEPHALUS (OMIM:276950)
VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS (OMIM:314390)
VACTERL with hydrocephalus (Orphanet:3412)
VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE (OMIM:219730)
VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY (OMIM:602200)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Von Hippel-Lindau disease (Orphanet:892)
Walker-Warburg syndrome (Orphanet:899)
Whipple disease (Orphanet:3452)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked centronuclear myopathy (Orphanet:596)
X-linked complicated corpus callosum dysgenesis (Orphanet:1497)
X-linked complicated spastic paraplegia type 1 (Orphanet:306617)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type (Orphanet:163966)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)