Preferred Name

BARDET-BIEDL SYNDROME 7

Synonyms

BBS7

ID

http://purl.bioontology.org/ontology/OMIM/615984

altLabel

BBS7

cui

C1859565

Gene Locus

4q27

Gene Symbol

BBS7

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU047527

http://purl.bioontology.org/ontology/OMIM/MTHU006627

http://purl.bioontology.org/ontology/OMIM/MTHU000133

http://purl.bioontology.org/ontology/OMIM/MTHU000250

http://purl.bioontology.org/ontology/OMIM/MTHU007674

http://purl.bioontology.org/ontology/OMIM/MTHU000322

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

615984

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

BARDET-BIEDL SYNDROME 7

Scope Statement

Limited clinical information provided on patients with BBS7 mutations [MISCELLANEOUS]

Caused by mutation in the BBS7 gene (BBS7, 607590.0001) [MOLECULAR BASIS]

tui

T047

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0110129 Human Disease Ontology / 人类疾病本体 LOOM
http://www.orpha.net/ORDO/Orphanet_118990 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0014435 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/MESH/C565916 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/C565916 Medical Subject Headings / 医学主题词表 LOOM
http://www.ebi.ac.uk/efo/EFO_0009026 Experimental Factor Ontology / 实验性因素本体 LOOM