SC phocomelia syndrome

Summary

SC phocomelia syndrome is a rare disease^[1].

Key Facts

• SC phocomelia syndrome's instance of is recorded as rare disease^[2].
• SC phocomelia syndrome's subclass of is recorded as autosomal recessive disease^[3].
• SC phocomelia syndrome's subclass of is recorded as phocomelia^[4].
• SC phocomelia syndrome's OMIM ID is recorded as 269000^[5].
• SC phocomelia syndrome's NCI Thesaurus ID is recorded as C4681^[6].
• SC phocomelia syndrome's genetic association is recorded as ESCO2^[7].
• SC phocomelia syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3103^[8].
• SC phocomelia syndrome's UMLS CUI is recorded as C0392475^[9].
• SC phocomelia syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[10].
• SC phocomelia syndrome's Mondo ID is recorded as MONDO_0010009^[11].