BASAN syndrome

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Summary

Literature (0)

DOID:0080725 - BASAN syndrome

Disease Ontology Definition:An ectodermal dysplasia that is characterized by neonatal blisters and milia and congenital absence of dermatoglyphics on the hands and feet.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: smarcad1

MIM:

MIM:129200 - BASAN SYNDROME

MIM:129200 - BASAN SYNDROME

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): ectodermal dysplasia (is_a)