Disease #01132 (PBD-14B;PEX-14B (peroxisome biogenesis disorder, type 14B (PBD-14B, PEX-14B)), OMIM:614920)

Official abbreviation PBD-14B;PEX-14B
Name peroxisome biogenesis disorder, type 14B (PBD-14B, PEX-14B)
OMIM ID 614920
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PEX11B
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Individuals

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00081035 - Trujillano et al., submitted unaffected parents - - - - - 0 - - PBD-14B;PEX-14B Peroxisome biogenesis disorder 14B (OMIM:614920) PEX11B PEX11B 1 1 Daniel Trujillano
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