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's subclass of is recorded as brachydactyly^[5].
• Liebenberg syndrome's subclass of is recorded as syndrome with brachydactyly^[6].
• Liebenberg syndrome's MeSH descriptor ID is recorded as C566090^[7].
• Liebenberg syndrome's OMIM ID is recorded as 186550^[8].
• Liebenberg syndrome's Orphanet ID is recorded as 1275^[9].
• Liebenberg syndrome's genetic association is recorded as PITX1^[10].
• Liebenberg syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1275^[11].
• Liebenberg syndrome's UMLS CUI is recorded as C1861313^[12].
• Liebenberg syndrome's ICD-10-CM is recorded as Q73.8^[13].
• Liebenberg syndrome's GARD rare disease ID is recorded as 966^[14].
• Liebenberg syndrome's Mondo ID is recorded as MONDO_0008520^[15].
• Liebenberg syndrome's Microsoft Academic ID is recorded as 2778873132^[16].
• Liebenberg syndrome's Genetics Home Reference Conditions ID is recorded as liebenberg-syndrome^[17].
• Liebenberg syndrome's UniProt disease ID is recorded as DI-03623^[18].