Bardet-biedl syndrome 4

Preferred Label : Bardet-biedl syndrome 4;

Symbol : BBS4;

CISMeF acronym : BBS4;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the BBS4 gene (BBS4, 600374.0001);

Prefixed ID : #615982;

Details

Origin ID

615982;

UMLS CUI

C2936864;

Automatic exact mappings (from CISMeF team)
- Bardet-Biedl syndrome 4 [DO Concept]
- Bardet-Biedl syndrome 4 [ORDO Gene]
- Bardet-Biedl syndrome 4 [MeSH concept]
- Bardet-Biedl syndrome 4 [HGNC gene]
- Bardet-Biedl syndrome 4 [MeSH Supplementary Concept]
DO Cross reference
- Bardet-Biedl syndrome 4 [DO Concept]
Genes related to phenotype
- Bbs4 gene [OMIM gene]
HPO term(s)
- Abnormality of the dentition [HPO term]
- Abnormality of the kidney [HPO term]
- Autosomal recessive inheritance [HPO term]
- Brachydactyly [HPO term]
- Cryptorchidism [HPO term]
- External genital hypoplasia [HPO term]
- Hypogonadism [HPO term]
- Intellectual disability [HPO term]
- Nyctalopia [HPO term]
- Obesity [HPO term]
- Polydactyly [HPO term]
- Renal cyst [HPO term]
- Retinal degeneration [HPO term]
- Rod-cone dystrophy [HPO term]
- Syndactyly [HPO term]
ORDO concept(s)
- Bardet-Biedl syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Bardet-Biedl syndrome 4 [DO Concept]
- Bardet-Biedl syndrome 4 [MeSH concept]
- Bardet-Biedl syndrome 4 [MeSH Supplementary Concept]
- Bardet-Biedl syndrome 4 [ORDO Gene]

Keyword's position in hierarchy(ies) :

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