Fibula shortening
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Database Frequency: | 3 / 7739 | |||
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All diseases associated with this symptom:
CHROMOSOME 2q31.1 DUPLICATION SYNDROME | (OMIM:613681) |
MESOMELIC DYSPLASIA, KANTAPUTRA TYPE | (OMIM:156232) |
SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION | (OMIM:612447) |