Central hypotonia

Symptom Information:

Symptom ID: HPO:0011398
Synonyms:
Central hypotonia [OMIM:Central hypotonia]
Quality:
Cross references:
OMIM: "Central hypotonia" [OMIM:Central hypotonia]
Is a (Direct Parents):
HPO         Abnormality of central motor function
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of central motor function(HPO:0011442)
                Central hypotonia(HPO:0011398)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Cataract-congenital heart disease-neural tube defect syndrome (Orphanet:314993)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15 (OMIM:615006)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Intellectual deficit, X-linked, Kroes type (Orphanet:163961)
Joubert syndrome 5 (OMIM:610188)
KABUKI SYNDROME 2 (OMIM:300867)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
PEROXISOME BIOGENESIS DISORDER 11B (OMIM:614885)
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) (OMIM:614886)
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) (OMIM:614887)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)