Fetal akinesia sequence
Symptom Information:
Symptom ID: | HPO:0001989 | ||||||
Synonyms: |
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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) Decreased fetal movement(HPO:0001558) Fetal akinesia sequence(HPO:0001989) MedDRA: |
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Database Frequency: | 14 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2 | (OMIM:615282) |
Congenital lethal myopathy, Compton-North type | (Orphanet:210163) |
FETAL AKINESIA SYNDROME, X-LINKED | (OMIM:300073) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Gaucher disease type 2 | (Orphanet:77260) |
LETHAL CONGENITAL CONTRACTURE SYNDROME 7 | (OMIM:616286) |
Lethal arthrogryposis - anterior horn cell disease | (Orphanet:53696) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Lissencephaly type 3 - metacarpal bone dysplasia | (Orphanet:86822) |
Metatropic dysplasia | (Orphanet:2635) |
Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
NEMALINE MYOPATHY 8 | (OMIM:615348) |
NEMALINE MYOPATHY 9 | (OMIM:615731) |
X-linked lethal multiple pterygium syndrome | (Orphanet:79447) |