Disease #00871 (CED2 (dysplasia, cranioectodermal, type 2 (CED-2)), OMIM:613610)

Official abbreviation CED2
Name dysplasia, cranioectodermal, type 2 (CED-2)
OMIM ID 613610
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 1
Associated with 1 gene WDR35
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

4 entries on 1 page. Showing entries 1 - 4.
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00320364 - - - M - Poland - - - - - CED2 - - WDR35 2 1 Joanna Walczak-Sztulpa
00320365 - - - M no Poland - 00y04m - - - CED2 - WDR35 WDR35 2 1 Joanna Walczak-Sztulpa
00320367 - - - F no Poland - - - - - CED2 - WDR35 WDR35 2 1 Joanna Walczak-Sztulpa
00320368 - - - F - Poland - - - - - CED2 - WDR35 WDR35 2 1 Joanna Walczak-Sztulpa
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