Term Name: Laurin-Sandrow syndrome
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
Definition: 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 (less than 80kb) duplications in a SHH regulatory element located in intron 5 of the LMBR1 gene on chromosome 7q36.3.
Ontology: Human Disease [DOID:0111350]   ( DOID:0111350 )

Relationships
is a type of: autosomal dominant disease dysostosis