Disease #04421 (UCMD2 (dystrophy, muscular, congenital, Ullrich, type 2?, (UCMD-2)), OMIM:616470)

Official abbreviation UCMD2
Name dystrophy, muscular, congenital, Ullrich, type 2?, (UCMD-2)
OMIM ID 616470
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene COL12A1
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Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00457300 - PubMed: İpek 2024 - F yes Turkey - - - - - UCMD2 IUGR (HP:0001511); joint hypermobility (HP:0001382); frequent falls (HP:0002359); delayed gross motor development (HP:0002194 ); high palate (HP:0000218); distal joint hypermobility (HP:0020152); finger joint contracture (HP:0034681); pes planus (HP:0001763); dry skin (HP:0000958); keratosis pilaris (HP:0032152); limb muscle weakness (HP:0003690). - COL12A1 1 1 Deepak Subramanian
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