Neurofibromatosis, type iv, of riccardi

Preferred Label : Neurofibromatosis, type iv, of riccardi;

Symbol : NF4;

CISMeF acronym : NF4;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Nf iv; Neurofibromatosis, variant form(s) of; Neurofibromatosis, atypical;

Inheritance : Autosomal dominant; heterogeneous;

Prefixed ID : 162270;

Details

Origin ID

162270;

UMLS CUI

C0220695;

Automatic exact mappings (from CISMeF team)
- Neurofibromatosis, type 4, of Riccardi [MeSH concept]
- neurofibromatosis [DO Concept]
- neurofibromatosis, type 4, of riccardi [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Atypical neurofibromatosis [HPO term]
HPO term(s)
- Atypical neurofibromatosis [HPO term]
- Autosomal dominant inheritance [HPO term]
- Heterogeneous [HPO term]
- Lisch nodules [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atypical neurofibromatosis [HPO term]
- Neurofibromatosis, type 4, of Riccardi [MeSH concept]
- neurofibromatosis, type 4, of riccardi [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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