Prenatal movement abnormality
Symptom Information:
Symptom ID: | HPO:0001557 | ||||
Synonyms: |
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Quality: | |||||
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) Prenatal movement abnormality(HPO:0001557) MedDRA: |
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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) |