Bifid nose, autosomal dominant

Preferred Label : Bifid nose, autosomal dominant;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ? also a recessive form (210400); Autosomal dominant form;

Prefixed ID : 109740;

Details

Origin ID

109740;

UMLS CUI

C2751431;

Broader ORDO disease(s)
- Bifid nose [ORDO Disease]
Currated CISMeF NLP mapping
- bifid nose, autosomal dominant [MeSH concept]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Autosomal dominant inheritance [HPO term]
- Bifid nose [HPO term]
- Cryptorchidism [HPO term]
- Midline defect of the nose [HPO term]
- Ptosis [HPO term]
- Usually autosomal dominant [HPO term]
Not associated HPO term(s)
- Hypertelorism [HPO term]
ORDO concept(s)
- Bifid nose [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- bifid nose, autosomal dominant [MeSH concept]

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