Renal, genital, and middle ear anomalies

Preferred Label : Renal, genital, and middle ear anomalies;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 267400;

Details

Origin ID

267400;

UMLS CUI

C1849432;

Currated CISMeF NLP mapping
- Renal-genital-middle ear anomalies [ORDO Disease]
- renal, genital, and middle ear anomalies [MeSH concept]
- renal, genital, and middle ear anomalies [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the middle ear ossicles [HPO term]
- Autosomal recessive inheritance [HPO term]
- Hearing impairment [HPO term]
- Renal hypoplasia/aplasia [HPO term]
- Vaginal atresia [HPO term]
ORDO concept(s)
- Renal-genital-middle ear anomalies [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Renal-genital-middle ear anomalies [ORDO Disease]
- renal, genital, and middle ear anomalies [MeSH Supplementary Concept]
- renal, genital, and middle ear anomalies [MeSH concept]

Keyword's position in hierarchy(ies) :

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