Disease #01726 (dysplasia, cranioectodermal, type 1, OMIM:218330)

Official abbreviation -
Name dysplasia, cranioectodermal, type 1
OMIM ID 218330
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 7
Associated with 1 gene IFT122
Associated tissues -
Disease features -
Remarks -


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00245400 - - - M - ? (unknown) - - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
00245401 - - - M - ? (unknown) - - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
00245402 - - - M - ? (unknown) - - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
00245403 - - - M - ? (unknown) - - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
00245404 - - - F - ? (unknown) Polish - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
00245405 - - - F - ? (unknown) Polish - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
00245406 - - - M - ? (unknown) Polish - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
00245407 - - - M - ? (unknown) Polish - 0 - - dysplasia, cranioectodermal, type 1 - IFT122 IFT122 1 1 LOVD
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