Short lower limbs

Symptom Information:

Symptom ID: HPO:0006385
Synonyms:
Short legs [HPO:0006385]
Short legs [OMIM:Short legs]
Short lower limbs [OMIM:Short lower limbs]
Short leg [OMIM:Short leg]
Quality:
Cross references:
OMIM: "Short legs" [OMIM:Short legs]
OMIM: "Short lower limbs" [OMIM:Short lower limbs]
OMIM: "Short leg" [OMIM:Short leg]
Is a (Direct Parents):
HPO         Lower limb undergrowth
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)
             Aplasia/hypoplasia involving the skeleton(HPO:0009115)
                Aplasia/hypoplasia of the extremities(HPO:0009815)
                   Limb undergrowth(HPO:0009826)
                      Lower limb undergrowth(HPO:0009816)
                         Short lower limbs(HPO:0006385)
                   Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                      Lower limb undergrowth(HPO:0009816)
                         Short lower limbs(HPO:0006385)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Aplasia/hypoplasia of the extremities(HPO:0009815)
                      Limb undergrowth(HPO:0009826)
                         Lower limb undergrowth(HPO:0009816)
                            Short lower limbs(HPO:0006385)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Lower limb undergrowth(HPO:0009816)
                            Short lower limbs(HPO:0006385)
                   Abnormality of the lower limb(HPO:0002814)
                      Aplasia/hypoplasia involving bones of the lower limbs(HPO:0006493)
                         Lower limb undergrowth(HPO:0009816)
                            Short lower limbs(HPO:0006385)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Cutis marmorata telangiectatica congenita (Orphanet:1556)
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES (OMIM:127200)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
MULTIPLE SYNOSTOSES SYNDROME 1 (OMIM:186500)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Multiple synostoses syndrome (Orphanet:3237)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)