neuroectodermal-endocrine syndrome
MONDO:0017045Mondo
Findings
No curated finding names neuroectodermal-endocrine syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0017045), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: neuroectodermal-endocrine syndrome
- Also called
- Oerter-Friedman-Anderson syndrome