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MIM:618019 - RHIZOMELIC SKELETAL DYSPLASIA WITH OR WITHOUT PELGER-HUET ANOMALY; SKPHA
Xenbase Genes: lbr
Human Disease Resource: OMIM
MONDO:0018663 - regressive spondylometaphyseal dysplasia |
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MONDO:0018663 - regressive spondylometaphyseal dysplasia |