Disease #01709 (RCDP-1 (chondrodysplasia punctata, rhizomelic, type 1 (RCDP-1)), OMIM:215100)

Official abbreviation RCDP-1
Name chondrodysplasia punctata, rhizomelic, type 1 (RCDP-1)
OMIM ID 215100
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PEX7
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Individuals

1 entry on 1 page. Showing entry 1.
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00132076 1 - - M ? ? (unknown) - - 0 - - RCDP-1 - ARSE, EBP, LBR, PEX7 PEX7 2 1 Karina Silveira
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