Neuroectodermal-endocrine syndrome
MONDO:0017045Neuroectodermal-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.
Also known as: Oerter-Friedman-Anderson syndrome, neuroectodermal endocrine syndrome
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Disease
(680)
Endocrine system disorder
(72)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
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Disorder of development or morphogenesis
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Polyendocrinopathy
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