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Familial isolated pituitary adenoma
2 OMIM references -
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Acromegaly
Giant cell glioblastoma
Gliosarcoma
Primary ciliary dyskinesia
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Chronic mucocutaneous candidiasis
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Pseudohyperaldosteronism type 2
Renal pseudohypoaldosteronism type 1
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Hereditary pheochromocytoma-paraganglioma
Synonym(s):
- FIPA
Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
AIP O00170605555
No signs/symptoms info available.