Disease #05256 (STHAG9 (agenesis, tooth, selective, type 9 (STHAG-9)), OMIM:617275)

Official abbreviation STHAG9
Name agenesis, tooth, selective, type 9 (STHAG-9)
OMIM ID 617275
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GREM2
Associated tissues -
Disease features -
Remarks -
Date created 2017-03-31 14:15:27 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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