Polyhydramnios

Symptom Information:

Symptom ID: HPO:0001561
Synonyms:
Hydramnios [HPO:0001561]
Polyhydramnios (disorder) [Orphanet:55060]
Polyhydramnios [Orphanet:55060]
Hydramnios [OMIM:Hydramnios]
Polyhydramnios [OMIM:Polyhydramnios]
Polyhydramnios [MedDRA:10036079]
Hydramnios [MedDRA:10036079]
Polyhydramnios affecting fetus or newborn [MedDRA:10036079]
Polyhydramnios, antepartum complication [MedDRA:10036079]
Polyhydramnios, unspecified as to episode of care [MedDRA:10036079]
Polyhydramnios, with delivery [MedDRA:10036079]
Polyhydramnios (36%) [OMIM:Polyhydramnios (36%)]
Polyhydramnios (congenital form) [OMIM:Polyhydramnios (congenital form)]
Polyhydramnios (in perinatal or congenital neuromuscular forms) [OMIM:Polyhydramnios (in perinatal or congenital neuromuscular forms)]
Polyhydramnios (severe form) [OMIM:Polyhydramnios (severe form)]
Quality:
Cross references:
Orphanet:55060 "Polyhydramnios" [Orphanet:55060]
OMIM: "Hydramnios" [OMIM:Hydramnios]
OMIM: "Polyhydramnios" [OMIM:Polyhydramnios]
OMIM: "Polyhydramnios (36%)" [OMIM:Polyhydramnios (36%)]
OMIM: "Polyhydramnios (congenital form)" [OMIM:Polyhydramnios (congenital form)]
OMIM: "Polyhydramnios (in perinatal or congenital neuromuscular forms)" [OMIM:Polyhydramnios (in perinatal or congenital neuromuscular forms)]
OMIM: "Polyhydramnios (severe form)" [OMIM:Polyhydramnios (severe form)]
UMLS:C0020224 "Hydramnios" [HPO:0001561]
UMLS:C0020224 "Polyhydramnios" [Orphanet:55060]
Is a (Direct Parents):
Orphanet Abnormality of prenatal development or birth
HPO         Abnormality of the amniotic fluid
MedDRA Amniotic fluid and cavity disorders of pregnancy NEC
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)
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)