CEDNIK syndrome

Summary

CEDNIK syndrome is a rare disease^[1].

Key Facts

• CEDNIK syndrome's instance of is recorded as rare disease^[2].
• CEDNIK syndrome's instance of is recorded as class of disease^[3].
• CEDNIK syndrome's subclass of is recorded as autosomal recessive disease^[4].
• CEDNIK syndrome's subclass of is recorded as genetic syndromic intellectual disability^[5].
• CEDNIK syndrome's subclass of is recorded as autosomal ichthyosis syndrome with fatal disease course^[6].
• CEDNIK syndrome's subclass of is recorded as syndrome^[7].
• CEDNIK syndrome's MeSH descriptor ID is recorded as C537943^[8].
• CEDNIK syndrome's OMIM ID is recorded as 609528^[9].
• CEDNIK syndrome's KEGG ID is recorded as H00799^[10].
• CEDNIK syndrome's Disease Ontology ID is recorded as DOID:0060337^[11].
• CEDNIK syndrome's Orphanet ID is recorded as 66631^[12].
• CEDNIK syndrome's health specialty is recorded as dermatology^[13].
• CEDNIK syndrome's genetic association is recorded as SNAP29^[14].
• CEDNIK syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060337^[15].
• CEDNIK syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060337^[16].
• CEDNIK syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_66631^[17].
• CEDNIK syndrome's UMLS CUI is recorded as C1836033^[18].
• CEDNIK syndrome's ICD-10-CM is recorded as Q82.8^[19].
• CEDNIK syndrome's GARD rare disease ID is recorded as 9940^[20].
• CEDNIK syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[21].
• CEDNIK syndrome's Mondo ID is recorded as MONDO_0012290^[22].
• CEDNIK syndrome's ICD-11 ID is recorded as 170763135^[23].
• CEDNIK syndrome's WikiProjectMed ID is recorded as CEDNIK syndrome^[24].
• CEDNIK syndrome's UniProt disease ID is recorded as DI-00251^[25].