Disease #01535 (PTOS1 (ptosis, hereditary congenital, type 1 (PTOS1)), OMIM:178300)

Official abbreviation PTOS1
Name ptosis, hereditary congenital, type 1 (PTOS1)
OMIM ID 178300
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ZFHX4
Associated tissues -
Disease features -
Remarks -