Disease #05234 (CM1 (malformation, Chiari, type I (CM-1)), OMIM:118420)

Official abbreviation CM1
Name malformation, Chiari, type I (CM-1)
OMIM ID 118420
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2017-03-06 20:17:57 +01:00 (CET)
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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00100621 @VED - - F no Italy White - - - Surgery of cranial posterior fossa CM1 - DKK1, FBN3, ITGA10, MATN3 DKK1, FBN3, ITGA10, MATN3 4 3 Patrizia De Marco
00100647 @DRN - - M no (Italy) white - - yes surgery of cranial posterior fossa CM1 hypertelorism, prominent head, epicanthus, clinodactyly, psycho-motor delay BMP1, EXT2, LRP4 BMP1, EXT2, LRP4 3 2 Patrizia De Marco
00100655 #MC - - F no (Italy) white - - yes surgery of cranial posterior fossa CM1 syringomyelia DKK1 DKK1 1 1 Patrizia De Marco
00100656 #CA - - M no (Italy) white - - - surgery of cranial posterior fossa CM1 cerebellar lipoma, hydrocephalus DKK1 DKK1 1 1 Patrizia De Marco
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