Details of Disease | DrugMAP

General Information of Disease (ID: DIS7D9VT)

Disease Name	Pituitary hormone deficiency, combined or isolated, 8
Disease Hierarchy	DISW6YL6: Combined pituitary hormone deficiencies, genetic form DIS7D9VT: Pituitary hormone deficiency, combined or isolated, 8
Disease Identifiers	MONDO ID MONDO_0957208 UMLS CUI C5830375 OMIM ID 620303 MedGen ID 1841011

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
ROBO1	TTND1YP	Strong	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ROBO1	OT52UFVS	Strong	Autosomal dominant	[1]
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References

1	Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain. Development. 2006 Jun;133(11):2243-52. doi: 10.1242/dev.02379.