A dysostosis characterized by polysyndactyly of hands and/or feet, mirror image duplication of the feet, nasal defects, and loss of identity between fibula and tibia that has_material_basis_in heterozygous inheritance of small (<80kb) duplications in a SHH regulatory element located in intron 5 of LMBR1 on chromosome 7q36.3.
Synonyms
miccor hands and feet with nasal defects,
MIPduplication of fibuland ulna with absence of tibia and radius,
mirror hands and feets-nasal defects syndrome,
mirror-image polydactyly,
Sandrow syndrome,
tetramelic mirror-image polydactyly,
TMIP
Click on a Disease Ontology term to go to its specific page within SGD; drag any of the Disease Ontology term objects around within the visualization
for easier viewing; click “Reset” to automatically redraw the diagram.