Prenatal movement abnormality

Symptom Information:

Symptom ID: HPO:0001557
Synonyms:
Abnormal intrauterine movements [HPO:0001557]
Abnormal fetal movement [Orphanet:55080]
Abnormal intrauterine movements [OMIM:Abnormal intrauterine movements]
Fetal immobility/abnormal fetal movements [Orphanet:55080]
Quality:
Cross references:
Orphanet:55080 "Fetal immobility/abnormal fetal movements" [Orphanet:55080]
OMIM: "Abnormal intrauterine movements" [OMIM:Abnormal intrauterine movements]
Is a (Direct Parents):
HPO         Abnormality of prenatal development or birth
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)
          Prenatal movement abnormality(HPO:0001557)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

14q22q23 microdeletion syndrome (Orphanet:264200)
2p21 microdeletion syndrome (Orphanet:163693)
Amish lethal microcephaly (Orphanet:99742)
Cohen syndrome (Orphanet:193)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Cornelia de Lange syndrome (Orphanet:199)
Fetal akinesia deformation sequence (Orphanet:994)
Freeman-Sheldon syndrome (Orphanet:2053)
Haddad syndrome (Orphanet:99803)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Neu-Laxova syndrome (Orphanet:2671)
Pyridoxine-dependent epilepsy (Orphanet:3006)
Schwartz-Jampel syndrome (Orphanet:800)
Smith-Magenis syndrome (Orphanet:819)
Wolf-Hirschhorn syndrome (Orphanet:280)