Disease #06648 (AMC2 (arthrogryposis multiplex congenita, type 2, neurogenic), OMIM:208100)

Official abbreviation AMC2
Name arthrogryposis multiplex congenita, type 2, neurogenic
OMIM ID 208100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease -
Associated with 1 gene ERGIC1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2024-10-01 09:43:19 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00398811 Individual A1 - - - - - - - - - - AMC2 - - COL25A1 1 1 Daniel Natera-de Benito
00398812 Patient B1 - - - - - - - - - - AMC2 - - COL25A1 1 1 Daniel Natera-de Benito
00398813 Patient C1 - - - - - - - - - - AMC2 - - COL25A1 2 1 Daniel Natera-de Benito
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