Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

PEROXISOME BIOGENESIS DISORDER 9B
Synonyms

PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP R
ID

http://purl.bioontology.org/ontology/OMIM/614879
altLabel

PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP R

PEROXISOME BIOGENESIS DISORDER, PEX7-RELATED, ATYPICAL

REFSUM DISEASE, ADULT, 2

PBD9B

PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 11

CGR

CG11
cui

C1866352

C1866351

C2749346
Gene Locus

6q23.3
Gene Symbol

PBD9B

PEX7

RCDP1
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

614879
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

PEROXISOME BIOGENESIS DISORDER 9B
tui

T047
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http://purl.bioontology.org/ontology/MESH/C567603 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C566635 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C566634 Medical Subject Headings CUI