Showing entry for Fingerprints, Absence of

General Disease Information
BXGD Id	BXGD015263
Disease Name	Fingerprints, Absence of
Disease CUI Id	C1852150
MeSH Codes	C16   C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0001574
Human Phenotype Ontology Term	Abnormality of the integument
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations