Cytoscape Web
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HESX1
5 associated diseases
1 protein interaction
UniProt info -
OMIM info -
Disease ODCs link
Combined pituitary hormone deficiencies, genetic forms
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Kallmann syndrome
Pituitary stalk interruption syndrome
Septo-optic dysplasia
Gene symbol Score
(click on to see the evidence)
PROP10.52