Disease #04422 (BTHLM2 (myopathy, Bethlem, type 2 (BTHLM-2)), OMIM:616471)

Official abbreviation BTHLM2
Name myopathy, Bethlem, type 2 (BTHLM-2)
OMIM ID 616471
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene COL12A1
Associated tissues -
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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00457407 - PubMed: El Sherif 2024 Muscle biopsy showed mild to moderate endomysial fibrosis and absent staining in collagen XII. F yes (Egypt) - - - - - BTHLM2 Motor delay (HP:0001270); neonatal hypotonia (HP:0001319); decreased fetal movement (HP:0001558); intrauterine growth retardation (HP:0001511); oligohydramnios (HP:0001562); high, narrow palate (HP:0002705); hyperextensible skin (HP:0000974); palmoplantar cutis laxa (HP:0007517); pectus excavatum (HP:0000767); neck muscle weakness (HP:0000467); kyphoscoliosis (HP:0002751); bilateral knee contractures (HP:0034671); distal joint hypermobility (HP:0020152); respiratory insufficiency due to muscle weakness (HP:0002747); pelvic girdle muscle atrophy (HP:0008988); proximal lower limb amyotrophy (HP:0008956); distal lower limb amyotrophy (HP:0008944); soft, doughy skin (HP:0001027). - COL12A1 1 1 Deepak Subramanian
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