Limb hypertonia

Symptom Information:

Symptom ID: HPO:0002509
Synonyms:
Limb hypertonia [OMIM:Limb hypertonia]
Hypertonia of the extremities [OMIM,du]
Quality:
Cross references:
OMIM: "Limb hypertonia" [OMIM:Limb hypertonia]
Is a (Direct Parents):
HPO         Abnormality of limb bone morphology
HPO         Hypertonia
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)
                Abnormal pyramidal signs(HPO:0007256)
                   Hypertonia(HPO:0001276)
                      Limb hypertonia(HPO:0002509)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Limb hypertonia(HPO:0002509)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Amish lethal microcephaly (Orphanet:99742)
Aromatic L-amino acid decarboxylase deficiency (Orphanet:35708)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21 (OMIM:615918)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
Dihydropteridine reductase deficiency (Orphanet:226)
Familial dyskinesia and facial myokymia (Orphanet:324588)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Gaucher disease type 2 (Orphanet:77260)
LISSENCEPHALY 6 WITH MICROCEPHALY (OMIM:616212)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B (OMIM:612389)
Propionic acidemia (Orphanet:35)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)