Hydrocephalus
Symptom Information:
Symptom ID: | HPO:0000238 | |||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||
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) Hydrocephalus(HPO:0000238) |
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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) |