Empty Sella Syndrome

Alias:
Empty Sella
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Empty Sella Syndrome, also known as empty sella, is related to premature ovarian failure 7 and intracranial hypertension, idiopathic. An important gene associated with Empty Sella Syndrome is PRL (Prolactin), and among its related pathways/superpathways are Signal Transduction and Translation Insulin regulation of translation. The drugs Insulin and Insulin, Globin Zinc have been mentioned in the context of this disorder. Affiliated tissues include pituitary and brain, and related phenotypes are nervous system and homeostasis/metabolism
Related ID:
MESH:D004652

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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13
131
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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IF
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