Disease #01726 (CED1 (dysplasia, cranioectodermal, type 1), OMIM:218330)

Official abbreviation CED1
Name dysplasia, cranioectodermal, type 1
OMIM ID 218330
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 7
Associated with 1 gene IFT122
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00245400 - - - M - - - - - - - CED1 - IFT122 IFT122 1 1 LOVD
00245401 - - - M - - - - - - - CED1 - IFT122 IFT122 1 1 LOVD
00245402 - - - M - - - - - - - CED1 - IFT122 IFT122 1 1 LOVD
00245403 - - - M - - - - - - - CED1 - IFT122 IFT122 1 1 LOVD
00245404 - - - F - - Polish - - - - CED1 - IFT122 IFT122 1 1 LOVD
00245405 - - - F - - Polish - - - - CED1 - IFT122 IFT122 1 1 LOVD
00245406 - - - M - - Polish - - - - CED1 - IFT122 IFT122 1 1 LOVD
00245407 - - - M - - Polish - - - - CED1 - IFT122 IFT122 1 1 LOVD
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