Pheochromocytoma--islet cell tumor syndrome

Preferred Label : Pheochromocytoma--islet cell tumor syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant; ? same as von Hippel-Lindau disease;

Prefixed ID : 171420;

Details

Origin ID

171420;

UMLS CUI

C1868392;

Automatic exact mappings (from CISMeF team)
- pheochromocytoma islet cell tumor syndrome [MeSH concept]
Currated CISMeF NLP mapping
- pheochromocytoma islet cell tumor syndrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Axillary freckling [HPO term]
- Cafe-au-lait spot [HPO term]
- Cerebral hemorrhage [HPO term]
- Congestive heart failure [HPO term]
- Elevated urinary norepinephrine [HPO term]
- Episodic hypertension [HPO term]
- Hypercalcemia [HPO term]
- Hyperhidrosis [HPO term]
- Hypertensive retinopathy [HPO term]
- Pheochromocytoma [HPO term]
- Positive regitine blocking test [HPO term]
- Proteinuria [HPO term]
- Tachycardia [HPO term]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- pheochromocytoma islet cell tumor syndrome [MeSH Supplementary Concept]
- pheochromocytoma islet cell tumor syndrome [MeSH concept]

Keyword's position in hierarchy(ies) :

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