Disease #06466 (ASGD6 (Anterior segment dysgenesis 6, multiple subtypes), OMIM:617315)

Official abbreviation ASGD6
Name Anterior segment dysgenesis 6, multiple subtypes
OMIM ID 617315
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CYP1B1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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