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Johnson neuroectodermal syndrome

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description Johnson neuroectodermal syndrome is characterised by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism.
Mondo Term and Equivalent IDs
MONDO:0007837:  Johnson neuroectodermal syndrome
GARD:0000378: 
MESH:C535882: 
Orphanet:2316: 
SCTID:721584005: 
UMLS:C0796002: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)
No novelty measurements found