Decreased fetal movement

Symptom Information:

Symptom ID: HPO:0001558
Synonyms:
Decreased fetal activity [HPO:0001558]
Decreased fetal movements [HPO:0001558]
Decreased movement in utero [HPO:0001558]
Reduced fetal movement [HPO:0001558]
Reduced fetal movements [HPO:0001558]
Reduced fetal movement (finding) [Orphanet:55080]
Reduced fetal movement [Orphanet:55080]
Decreased fetal movement [OMIM:Decreased fetal movement]
Decreased fetal movements [OMIM:Decreased fetal movements]
Decreased movement in utero [OMIM:Decreased movement in utero]
Reduced fetal movement [OMIM:Reduced fetal movement]
Reduced fetal movements [OMIM:Reduced fetal movements]
Fetal immobility/abnormal fetal movements [Orphanet:55080]
Fetal movements decreased [Orphanet:55080]
Foetal hypokinesia [MedDRA:10068461]
Foetal movements decreased [MedDRA:10068461]
Fetal movements decreased [MedDRA:10068461]
Fetal hypokinesia [MedDRA:10068461]
Decreased fetal movement (in perinatal or congenital neuromuscular forms) [OMIM:Decreased fetal movement (in perinatal or congenital neuromuscular forms)]
Decreased fetal movement (severe form) [OMIM:Decreased fetal movement (severe form)]
Decreased fetal movements (2p21del and HCS) [OMIM:Decreased fetal movements (2p21del and HCS)]
Decreased fetal movements (36%) [OMIM:Decreased fetal movements (36%)]
Decreased fetal movements (in some patients) [OMIM:Decreased fetal movements (in some patients)]
Decreased fetal movements (less common) [OMIM:Decreased fetal movements (less common)]
Decreased movements in utero (in some patients) [OMIM:Decreased movements in utero (in some patients)]
Fetal hypokinesia [OMIM:Fetal hypokinesia]
Reduced fetal movements (congenital form) [OMIM:Reduced fetal movements (congenital form)]
Quality:
Cross references:
Orphanet:55080 "Fetal immobility/abnormal fetal movements" [Orphanet:55080]
OMIM: "Decreased fetal movement" [OMIM:Decreased fetal movement]
OMIM: "Decreased fetal movements" [OMIM:Decreased fetal movements]
OMIM: "Decreased movement in utero" [OMIM:Decreased movement in utero]
OMIM: "Reduced fetal movement" [OMIM:Reduced fetal movement]
OMIM: "Reduced fetal movements" [OMIM:Reduced fetal movements]
OMIM: "Decreased fetal movement (in perinatal or congenital neuromuscular forms)" [OMIM:Decreased fetal movement (in perinatal or congenital neuromuscular forms)]
OMIM: "Decreased fetal movement (severe form)" [OMIM:Decreased fetal movement (severe form)]
OMIM: "Decreased fetal movements (2p21del and HCS)" [OMIM:Decreased fetal movements (2p21del and HCS)]
OMIM: "Decreased fetal movements (36%)" [OMIM:Decreased fetal movements (36%)]
OMIM: "Decreased fetal movements (in some patients)" [OMIM:Decreased fetal movements (in some patients)]
OMIM: "Decreased fetal movements (less common)" [OMIM:Decreased fetal movements (less common)]
OMIM: "Decreased movements in utero (in some patients)" [OMIM:Decreased movements in utero (in some patients)]
OMIM: "Fetal hypokinesia" [OMIM:Fetal hypokinesia]
OMIM: "Reduced fetal movements (congenital form)" [OMIM:Reduced fetal movements (congenital form)]
UMLS:C0235659 "Reduced fetal movement" [Orphanet:55080]
Is a (Direct Parents):
HPO         Prenatal movement abnormality
MedDRA Foetal complications NEC
Orphanet Abnormality of prenatal development or birth
Orphanet Prenatal movement abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of prenatal development or birth(HPO:0001197)
          Prenatal movement abnormality(HPO:0001557)
             Decreased fetal movement(HPO:0001558)
MedDRA:
Pregnancy, puerperium and perinatal conditions(MedDRA:10036585)
    Foetal complications(MedDRA:10016849)
       Foetal complications NEC(MedDRA:10016850)
          Decreased fetal movement(HPO:0001558)
Database Frequency: 74 / 7739
Resource:

All diseases associated with this symptom:

2p21 microdeletion syndrome (Orphanet:163693)
Adenylosuccinate lyase deficiency (Orphanet:46)
Antenatal multiminicore disease with arthrogryposis multiplex congenita (Orphanet:178148)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arthrogryposis multiplex congenita (Orphanet:1037)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Autosomal dominant congenital benign spinal muscular atrophy (Orphanet:1216)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Bethlem myopathy (Orphanet:610)
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 2 (OMIM:615119)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Congenital fiber-type disproportion myopathy (Orphanet:2020)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Congenital myopathy with excess of thin filaments (Orphanet:98904)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 (OMIM:615833)
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type (Orphanet:300179)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
FEINGOLD SYNDROME 1 (OMIM:164280)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Feingold syndrome (Orphanet:1305)
Fetal Gaucher disease (Orphanet:85212)
Fetal akinesia-cerebral and retinal hemorrhage syndrome (Orphanet:363409)
Gaucher disease type 2 (Orphanet:77260)
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)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
LETHAL CONGENITAL CONTRACTURE SYNDROME 6 (OMIM:616248)
Lethal congenital contracture syndrome type 2 (Orphanet:137776)
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect (Orphanet:330050)
Lethal restrictive dermopathy (Orphanet:1662)
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS (OMIM:604317)
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE (OMIM:609456)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 (OMIM:615351)
MUSCULAR HYPERTONIA, LETHAL (OMIM:254120)
MYASTHENIC SYNDROME, CONGENITAL, 10 (OMIM:254300)
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616326)
MYASTHENIC SYNDROME, CONGENITAL, 18 (OMIM:616330)
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL (OMIM:616322)
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:608931)
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET (OMIM:614399)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION (OMIM:255310)
Metatropic dysplasia (Orphanet:2635)
Miller-Dieker syndrome (Orphanet:531)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
NEMALINE MYOPATHY 10 (OMIM:616165)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEU-LAXOVA SYNDROME 2 (OMIM:616038)
Nemaline myopathy (Orphanet:607)
Neu-Laxova syndrome (Orphanet:2671)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Postsynaptic congenital myasthenic syndromes (Orphanet:98913)
Prader-Willi syndrome (Orphanet:739)
Proximal spinal muscular atrophy (Orphanet:70)
Proximal spinal muscular atrophy type 1 (Orphanet:83330)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Steinert myotonic dystrophy (Orphanet:273)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
TMCO1 defect syndrome (Orphanet:228407)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked centronuclear myopathy (Orphanet:596)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)