Fetal akinesia sequence

Symptom Information:

Symptom ID: HPO:0001989
Synonyms:
Early severe fetal akinesia sequence [HPO:0001989]
Fetal akinesia [HPO:0001989]
Early severe fetal akinesia sequence [OMIM:Early severe fetal akinesia sequence]
Fetal akinesia [OMIM:Fetal akinesia]
Fetal akinesia (in some patients) [OMIM:Fetal akinesia (in some patients)]
Fetal akinesia sequence (FAS) [OMIM:Fetal akinesia sequence (FAS)]
Quality:
Cross references:
OMIM: "Early severe fetal akinesia sequence" [OMIM:Early severe fetal akinesia sequence]
OMIM: "Fetal akinesia" [OMIM:Fetal akinesia]
OMIM: "Fetal akinesia (in some patients)" [OMIM:Fetal akinesia (in some patients)]
OMIM: "Fetal akinesia sequence (FAS)" [OMIM:Fetal akinesia sequence (FAS)]
Is a (Direct Parents):
HPO         Decreased fetal movement
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:
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)