Decreased fetal movement
Symptom Information:
Symptom ID: | HPO:0001558 | |||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||
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) |