C4510365_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	This syndrome has characteristics of the combination of endocrine and neuroectodermal abnormalities. These abnormalities include 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 siblings from Myanmar.
?:hasCUIAnnotation	<https://research.tib.eu/covid-19/entity/C4510365>
?:hasGeneratedBy	<https://research.tib.eu/covid-19/SourceName/SNOMEDCT_US>
?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

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