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DOID:0111877 - linear skin defects with multiple congenital anomalies 2
Disease Ontology Definition:A linear skin defects with multiple congenital anomalies characterized by linear skin defects, microcephaly, facial dysmorphism, and other congenital anomalies that has_material_basis_in heterozygous mutation in the COX7B gene on chromosome Xq21.1.
Synonyms: APLCC, LSDMCA2, aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
MLS syndrome (is_a),
physical disorder (is_a)