Disease #00532 (CCMS (cerebro-cosot-mandibular syndrome (CCMS)), OMIM:117650)

Official abbreviation CCMS
Name cerebro-cosot-mandibular syndrome (CCMS)
OMIM ID 117650
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene SNRPB
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-21 11:44:36 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00019874 - - - M - - - - - - - CCMS - SNRPB SNRPB 1 1 Céline Huber-Lequesne
00019875 - - - M - - - - - - - CCMS - SNRPB SNRPB 1 1 Céline Huber-Lequesne
00019876 - - - F - - - - - - - CCMS - SNRPB SNRPB 1 1 Céline Huber-Lequesne
00019877 - - - M - - - - - - - CCMS - SNRPB SNRPB 1 1 Céline Huber-Lequesne
00019878 - - - F - - - - - - - CCMS - SNRPB SNRPB 1 1 Céline Huber-Lequesne
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