Generalized neonatal hypotonia

Symptom Information:

Symptom ID: HPO:0008935
Synonyms:
Hypotonia, neonatal, generalized [HPO:0008935]
Hypotonia, neonatal, generalized [OMIM:Hypotonia, neonatal, generalized]
Quality:
Cross references:
OMIM: "Hypotonia, neonatal, generalized" [OMIM:Hypotonia, neonatal, generalized]
Is a (Direct Parents):
HPO         Neonatal hypotonia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Abnormal muscle tone(HPO:0003808)
                Muscular hypotonia(HPO:0001252)
                   Neonatal hypotonia(HPO:0001319)
                      Generalized neonatal hypotonia(HPO:0008935)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Combined oxidative phosphorylation defect type 4 (Orphanet:254925)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED (OMIM:300580)
PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER) (OMIM:614882)
PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER) (OMIM:614859)
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER) (OMIM:614862)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) (OMIM:614866)
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER) (OMIM:614870)
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER) (OMIM:614872)
PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER) (OMIM:614876)