Lower limb hypertonia

Symptom Information:

Symptom ID: HPO:0006895
Synonyms:
Lower limb hypertonia [OMIM:Lower limb hypertonia]
Quality:
Cross references:
OMIM: "Lower limb hypertonia" [OMIM:Lower limb hypertonia]
Is a (Direct Parents):
HPO         Limb hypertonia
HPO         Abnormality of the lower limb
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                   Abnormality of the lower limb(HPO:0002814)
                      Lower limb hypertonia(HPO:0006895)
                   Limb hypertonia(HPO:0002509)
                      Lower limb hypertonia(HPO:0006895)
       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)
                         Lower limb hypertonia(HPO:0006895)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive spastic paraplegia type 14 (Orphanet:100995)
PELGER-HUET ANOMALY (OMIM:169400)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)