Liebenberg syndrome
human disease
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Liebenberg syndrome
Summary
Liebenberg syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Liebenberg syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Liebenberg syndrome's instance of is recorded as rare disease[3].
- Liebenberg syndrome's instance of is recorded as class of disease[4].
- Liebenberg syndrome is a type of brachydactyly[5].
- Liebenberg syndrome is a type of syndrome with brachydactyly[6].
- Liebenberg syndrome's genetic association is recorded as PITX1[7].
- Liebenberg syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1275[8].