Disease #00667 (TRIGNO2 (trigonocephaly, type 2 (TRIGNO-2)), OMIM:614485)

Official abbreviation TRIGNO2
Name trigonocephaly, type 2 (TRIGNO-2)
OMIM ID 614485
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 0
Associated with 1 gene FREM1
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00247317 - - - - - - - - 0 - - TRIGNO2 - FREM1 FREM1 1 1 SIB - Livia Famiglietti
00247321 - - - - - - - - 0 - - TRIGNO2 - FREM1 FREM1 1 1 SIB - Livia Famiglietti
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