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autosomal recessive spondylometaphyseal dysplasia, Megarbane type

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any spondylodysplastic dysplasia in which the cause of the disease is a mutation in the PAM16 gene.
Uniprot Description An autosomal recessive disease characterized by pre- and postnatal short stature, developmental delay, dysmorphic facial appearance, narrow chest, prominent abdomen, platyspondyly, and short limbs.
Mondo Term and Equivalent IDs
MONDO:0013223:  autosomal recessive spondylometaphyseal dysplasia, Megarbane type
MESH:C567644: 
Orphanet:401979: 
UMLS:C2750075: