Disease #00653

Official abbreviation TRIGNO-1
Name trigonocephaly, type 1 (TRIGNO-1)
OMIM ID 190440
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FGFR1
Associated tissues -
Disease features -
Remarks -