Oligohydramnios
Symptom Information:
Symptom ID: | HPO:0001562 | ||||||||||||
Synonyms: |
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Cross references: |
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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) Oligohydramnios(HPO:0001562) 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) Oligohydramnios(HPO:0001562) |
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Database Frequency: | 75 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
46,XX disorder of sex development - anorectal anomalies | (Orphanet:2973) |
ADAMS-OLIVER SYNDROME 2 | (OMIM:614219) |
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA | (OMIM:613623) |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
Acro-renal-mandibular syndrome | (Orphanet:958) |
Amniotic bands | (Orphanet:1034) |
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis | (Orphanet:1112) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
BRESEK syndrome | (Orphanet:85284) |
Bilateral renal agenesis | (Orphanet:1848) |
COLE-CARPENTER SYNDROME 2 | (OMIM:616294) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA | (OMIM:219100) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Campomelia, Cumming type | (Orphanet:1318) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Congenital hydronephrosis | (Orphanet:2190) |
Craniosynostosis, Herrmann-Opitz type | (Orphanet:2145) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Familial caudal dysgenesis | (Orphanet:1768) |
Fanconi anemia | (Orphanet:84) |
Fetal Gaucher disease | (Orphanet:85212) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Haddad syndrome | (Orphanet:99803) |
Hb Bart's hydrops fetalis | (Orphanet:163596) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Indomethacin embryofetopathy | (Orphanet:1909) |
Leprechaunism | (Orphanet:508) |
Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
Lymphedema - atrial septal defects - facial changes | (Orphanet:86915) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 | (OMIM:257300) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 14 | (OMIM:615350) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Meckel syndrome, type 11 | (OMIM:615397) |
Meckel syndrome, type 12 | (OMIM:616258) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mosaic trisomy 9 | (Orphanet:99776) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
NPHP3-related Meckel-like syndrome | (Orphanet:3032) |
Neonatal hemochromatosis | (Orphanet:446) |
Nephronophthisis 2 | (OMIM:602088) |
Nephronophthisis 3 | (OMIM:604387) |
Neurogenic arthrogryposis multiplex congenita | (Orphanet:1143) |
Oculo-palato-cerebral syndrome | (Orphanet:2714) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Osteocraniostenosis | (Orphanet:2763) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES | (OMIM:602249) |
Paternal 20q13.2q13.3 microdeletion syndrome | (Orphanet:261304) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
Prune belly syndrome | (Orphanet:2970) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 | (OMIM:208540) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 | (OMIM:615415) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Radius absent - anogenital anomalies | (Orphanet:3016) |
Renal tubular dysgenesis | (Orphanet:3033) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
Spondylocostal dysostosis - anal and genitourinary malformations | (Orphanet:94095) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Thomas syndrome | (Orphanet:3316) |
Thrombocytopenia - Robin sequence | (Orphanet:3323) |
Thymic-renal-anal-lung dysplasia | (Orphanet:3326) |
Trisomy 18 | (Orphanet:3380) |
Ulbright-Hodes syndrome | (Orphanet:3404) |