The detail information of Ehlers-Danlos syndrome, classic-like, 1
OMIA Basic Information

Possible human homologues (MIM numbers):

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Recessive

Considered a defect: yes

Year key mutation first reported: 2019

Species-specific name: -

Species-specific symbol: -

More detail information can see in

Associated Breeds
There are associated breeds.
Associated Gene
There are no associated genes.
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
2019 Bauer,A.,deLucia,M.,Leuthard,F.,Jagannathan,V.,Leeb,T.,Bauer,A.,deLucia,M.,Leuthard,F.,Jagannathan,V.,Leeb,T.: :
Compound heterozygosity for TNXB genetic variants in a mixed-breed dog with Ehlers-Danlos syndrome. Anim Genet 50:546-549, 2019.
Pubmed reference: 31365140 . DOI: 10.1111/age.12830 .