Polyhydramnios
Symptom Information:
Symptom ID: | HPO:0001561 | |||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of prenatal development or birth(HPO:0001197) Abnormality of the amniotic fluid(HPO:0001560) Polyhydramnios(HPO:0001561) MedDRA: Pregnancy, puerperium and perinatal conditions(MedDRA:10036585) Placental, amniotic and cavity disorders (excl haemorrhages)(MedDRA:10035129) Amniotic fluid and cavity disorders of pregnancy NEC(MedDRA:10001970) Polyhydramnios(HPO:0001561) |
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Database Frequency: | 191 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
17q12 microduplication syndrome | (Orphanet:261272) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
Achondrogenesis | (Orphanet:932) |
Achondrogenesis type 1A | (Orphanet:93299) |
Achondrogenesis type 1B | (Orphanet:93298) |
Achondrogenesis type 2 | (Orphanet:93296) |
Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
Atelosteogenesis type I | (Orphanet:1190) |
Autosomal recessive amelia | (Orphanet:1027) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
BARTTER SYNDROME, TYPE 4A | (OMIM:602522) |
BARTTER SYNDROME, TYPE 4B | (OMIM:613090) |
Bamforth syndrome | (Orphanet:1226) |
Bartter syndrome | (Orphanet:112) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion | (Orphanet:231130) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Boomerang dysplasia | (Orphanet:1263) |
C syndrome | (Orphanet:1308) |
CAMPOMELIC DYSPLASIA | (OMIM:114290) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CHARGE syndrome | (Orphanet:138) |
CIRCUMVALLATE PLACENTA SYNDROME | (OMIM:215550) |
CODAS syndrome | (Orphanet:1458) |
Campomelic dysplasia | (Orphanet:140) |
Cardiocranial syndrome, Pfeiffer type | (Orphanet:2872) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Congenital chloride diarrhea | (Orphanet:53689) |
Congenital hydronephrosis | (Orphanet:2190) |
Congenital lethal myopathy, Compton-North type | (Orphanet:210163) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Congenital pulmonary airway malformation | (Orphanet:2444) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Congenital sodium diarrhea | (Orphanet:103908) |
Costello syndrome | (Orphanet:3071) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Duodenal atresia | (Orphanet:1203) |
Dysmorphism - conductive hearing loss - heart defect | (Orphanet:289553) |
Dysplastic cortical hyperostosis | (Orphanet:2204) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Epidermolysis bullosa simplex with pyloric atresia | (Orphanet:158684) |
FEINGOLD SYNDROME 1 | (OMIM:164280) |
FETAL AKINESIA DEFORMATION SEQUENCE | (OMIM:208150) |
FETAL AKINESIA SYNDROME, X-LINKED | (OMIM:300073) |
Familial visceral myopathy | (Orphanet:2604) |
Feingold syndrome | (Orphanet:1305) |
Fetal Gaucher disease | (Orphanet:85212) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Fetal akinesia-cerebral and retinal hemorrhage syndrome | (Orphanet:363409) |
Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
Fowler syndrome | (Orphanet:221126) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Fryns syndrome | (Orphanet:2059) |
Gaucher disease type 2 | (Orphanet:77260) |
Genitopatellar syndrome | (Orphanet:85201) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form | (Orphanet:308712) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form | (Orphanet:308684) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form | (Orphanet:308698) |
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form | (Orphanet:308670) |
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form | (Orphanet:308655) |
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form | (Orphanet:308638) |
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form | (Orphanet:308621) |
Greenberg dysplasia | (Orphanet:1426) |
HEC syndrome | (Orphanet:2119) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES | (OMIM:613124) |
Haddad syndrome | (Orphanet:99803) |
Hb Bart's hydrops fetalis | (Orphanet:163596) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
Hydrolethalus | (Orphanet:2189) |
Hypochondrogenesis | (Orphanet:93297) |
Hypomandibular faciocranial dysostosis | (Orphanet:1790) |
Hypotonia-cerebral atrophy-hyperglycinemia syndrome | (Orphanet:363424) |
Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
Infantile Bartter syndrome with deafness | (Orphanet:89938) |
Infantile hypophosphatasia | (Orphanet:247651) |
Iniencephaly | (Orphanet:63259) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
KAGAMI-OGATA SYNDROME | (OMIM:608149) |
Kenny-Caffey syndrome | (Orphanet:2333) |
LETHAL CONGENITAL CONTRACTURE SYNDROME 7 | (OMIM:616286) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
Lethal chondrodysplasia, Moerman type | (Orphanet:1420) |
Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
Lethal congenital contracture syndrome type 2 | (Orphanet:137776) |
Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Lissencephaly type 3 - metacarpal bone dysplasia | (Orphanet:86822) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED | (OMIM:300580) |
Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Methimazole embryofetopathy | (Orphanet:1923) |
Microlissencephaly - micromelia | (Orphanet:50810) |
Microphthalmia - microtia - fetal akinesia | (Orphanet:2547) |
Miller-Dieker syndrome | (Orphanet:531) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
Multiple intestinal atresia | (Orphanet:2300) |
NEMALINE MYOPATHY 10 | (OMIM:616165) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NOONAN SYNDROME 8 | (OMIM:615355) |
NPHP3-related Meckel-like syndrome | (Orphanet:3032) |
Nemaline myopathy | (Orphanet:607) |
Neonatal hemochromatosis | (Orphanet:446) |
Neu-Laxova syndrome | (Orphanet:2671) |
Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Opsismodysplasia | (Orphanet:2746) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
POLYHYDRAMNIOS, CHRONIC IDIOPATHIC | (OMIM:263610) |
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
PYLORIC ATRESIA | (OMIM:265950) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Perlman syndrome | (Orphanet:2849) |
Peters-plus syndrome | (Orphanet:709) |
Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
Polysyndactyly - cardiac malformation | (Orphanet:2934) |
Pontocerebellar hypoplasia type 4 | (Orphanet:166063) |
Proximal spinal muscular atrophy | (Orphanet:70) |
RADICULONEUROPATHY, FATAL NEONATAL | (OMIM:266250) |
ROBERTS SYNDROME | (OMIM:268300) |
Renal tubular dysgenesis | (Orphanet:3033) |
Ring chromosome 8 | (Orphanet:1450) |
Roberts syndrome | (Orphanet:3103) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SENER SYNDROME | (OMIM:606156) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Schneckenbecken dysplasia | (Orphanet:3144) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Senior-Loken syndrome 8 | (OMIM:616307) |
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 11 with or without polydactyly | (OMIM:615633) |
Short-rib thoracic dysplasia 8 with or without polydactyly | (OMIM:615503) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Spondylocostal dysostosis - anal and genitourinary malformations | (Orphanet:94095) |
Steinert myotonic dystrophy | (Orphanet:273) |
Symmetrical thalamic calcifications | (Orphanet:1314) |
Syndromic diarrhea | (Orphanet:84064) |
THANATOPHORIC DYSPLASIA, TYPE II | (OMIM:187601) |
TMCO1 defect syndrome | (Orphanet:228407) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
Tetraamelia - multiple malformations | (Orphanet:3301) |
Thanatophoric dysplasia | (Orphanet:2655) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
Thanatophoric dysplasia type 2 | (Orphanet:93274) |
Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |
Tracheal agenesis | (Orphanet:3346) |
Tracheo-esophageal fistula - hypospadias | (Orphanet:2042) |
Transaldolase deficiency | (Orphanet:101028) |
Triopia | (Orphanet:3374) |
Triploidy | (Orphanet:3376) |
Trisomy 1q | (Orphanet:261344) |
Umbilical cord ulceration - intestinal atresia | (Orphanet:3405) |
VACTERL with hydrocephalus | (Orphanet:3412) |
VACTERL/VATER association | (Orphanet:887) |
VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE | (OMIM:219730) |
VESICOURETERAL REFLUX 3 | (OMIM:613674) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
Wolfram syndrome 1 | (OMIM:222300) |
X-linked centronuclear myopathy | (Orphanet:596) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
X-linked lethal multiple pterygium syndrome | (Orphanet:79447) |
XK aprosencephaly | (Orphanet:3469) |
Yunis-Varon syndrome | (Orphanet:3472) |