type IV hypersensitivity disease autoimmune disease obsolete inflammatory and autoimmune disease with epilepsy obsolete systemic inflammatory disease associated with an acquired peripheral neuropathy non-familial restrictive cardiomyopathy obsolete systemic diseases with anterior uveitis obsolete systemic diseases with posterior uveitis obsolete systemic diseases with panuveitis sarcoidosis https://github.com/monarch-initiative/mondo/issues/6742 https://github.com/monarch-initiative/mondo/issues/6878 https://github.com/monarch-initiative/mondo/issues/9097 NCIT:C34995 Darier-Roussy sarcoid Editor note: ORDO makes this a type of cardiomyopathy but this would render the subclass cardiac sarcoidosis equivalent; same with neurogenic sarcoidosis. TODO - check type of hypersensitivity disease. This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'connective tissue disorder' (MONDO:0018153) ontology branch (https://orcid.org/0000-0002-1780-5230). ICD10CM:D86 NANDO:1200415 Boeck's sarcoidosis MedDRA:10039486 Boeck's sarcoid Boeck sarcoid GARD:0007607 sarcoidosis MESH:D012507 icd11.foundation:330792642 NORD:1690 MONDO:0019338 Sarcoidosis is a multisystemic disorder of unknown cause characterized by the formation of immune granulomas in involved organs. sarcoid DOID:11335 besnier-Boeck-Schaumann syndrome Orphanet:797 ICD10WHO:D86 SCTID:31541009 UMLS:C0036202 MEDGEN:48554 Besnier-Boeck-Schaumann disease obsolete secondary glomerular disease autoinflammatory syndrome obsolete pituitary hormone deficiency secondary to a granulomatous disease