Disease #02022

Official abbreviation ARPKD
Name kidney, polycystic, disease, autosomal recessive (ARPKD, infantile type)
OMIM ID 263200
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PKHD1
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Disease features -
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Individuals

1 entry on 1 page. Showing entry 1.
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00080834 - Trujillano et al., submitted unaffected parents - - - - - 0 - - ARPKD Polycystic kidney and hepatic disease (OMIM:263200) PKHD1 PKHD1 1 1 Daniel Trujillano
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