Normal high-resolution karyotype
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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HPO:
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Database Frequency: | 1 / 7739 | |
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All diseases associated with this symptom:
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |