Oligohydramnios

Symptom Information:

Symptom ID: HPO:0001562
Synonyms:
Maternal oligohydramnios [HPO:0001562]
Oligohydramnios (disorder) [Orphanet:55040]
Oligohydramnios [Orphanet:55040]
Oligohydramnios [OMIM:Oligohydramnios]
Oligoamnios [Orphanet:55040]
Oligohydramnios [MedDRA:10030289]
Oligohydramnios affecting fetus or newborn [MedDRA:10030289]
Oligohydramnios, antepartum [MedDRA:10030289]
Oligohydramnios, delivered [MedDRA:10030289]
Oligohydramnios, unspecified as to episode of care [MedDRA:10030289]
Anhydramnios [MedDRA:10030289]
Oligohydramnios (in some patients) [OMIM:Oligohydramnios (in some patients)]
Quality:
Cross references:
Orphanet:55040 "Oligoamnios" [Orphanet:55040]
OMIM: "Oligohydramnios" [OMIM:Oligohydramnios]
OMIM: "Oligohydramnios (in some patients)" [OMIM:Oligohydramnios (in some patients)]
UMLS:C0079924 "Oligohydramnios" [HPO:0001562]
UMLS:C0079924 "Oligohydramnios" [Orphanet:55040]
Is a (Direct Parents):
HPO         Abnormality of the amniotic fluid
MedDRA Amniotic fluid and cavity disorders of pregnancy NEC
Orphanet Abnormality of prenatal development or birth
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)
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)