syndromic intellectual disability polyendocrinopathy multiple congenital anomalies/dysmorphic syndrome-intellectual disability neuroectodermal-endocrine syndrome https://github.com/monarch-initiative/mondo/issues/5588 https://rarediseases.info.nih.gov/diseases/3959/neuroectodermal-endocrine-syndrome Orphanet:2676 SCTID:724090001 Oerter-Friedman-Anderson syndrome GARD:0003959 neuroectodermal endocrine syndrome Neuroectodermal-endocrine syndrome is characterized by a combination of endocrine and neuroectodermal abnormalities, including low growth hormone levels, delayed puberty, type II diabetes mellitus, mild intellectual deficit, sensorineural deafness, characteristic facial appearance and alopecia. It has been described in four sibs from Myanmar. MONDO:0017045