Disease #00666 (MOTA (Manitoba oculotrichoanal syndrome (MOTA)), OMIM:248450)

Official abbreviation MOTA
Name Manitoba oculotrichoanal syndrome (MOTA)
OMIM ID 248450
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 0
Associated with 1 gene FREM1
Associated tissues -
Disease features -
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00247319 - - - - - - - - 0 - - MOTA - FREM1 FREM1 1 1 SIB - Livia Famiglietti
00247322 - - - - - - - - 0 - - MOTA - FREM1 FREM1 1 1 SIB - Livia Famiglietti
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