Disease #03338

Official abbreviation -
Name dysplasia, frontonasal, type 3
OMIM ID 613456
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene ALX1
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00204588 - - - - yes Turkey - - 0 - - dysplasia, frontonasal, type 3 - ALX1 ALX1 1 1 -
00204589 - - parents distantly related - - Turkey - - 0 - - dysplasia, frontonasal, type 3 - ALX1 ALX1 1 1 -
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