Search Phenotypes

Achondrogenesis, type II — Holstein bull-dog dwarfism

In a remarkable indication of the power of whole-genome sequence analysis, Daetwyler et al. (2014) identified a causal mutation for this disorder in Holstein Friesian cattle as a missense mutation (g.32475732G>A [UMD3.1 reference sequence]; p.Gly960Arg, omia.variant:223) in the COL2A1 gene (which encodes the alpha-1 chain of type II collagen), by comparing the sequence of only two affected calves with sequence from bulls in the 1000-bull-ge...

OMIA ID: 1926Inheritance: 3Characterised: YesYear: 2014

Complex vertebral malformation — Haplotype HHC

Complex vertebral malformation is an inherited syndrome in Holstein-Friesian cattle. CVM has been reported in aborted, premature born, stillborn and neonatal calves. Affected calves have a reduced weight, a misshapen backbone and tendon contractions in the legs. Several other malformations including heart malformations are associated with this syndrome. A DNA test is available in Denmark and the Netherlands. [Imke Tammen: 26 Jan 2002] From a s...

OMIA ID: 1340Inheritance: 5Characterised: YesYear: 2006

Glycogen storage disease V — Myophosphorylase deficiency

The first occurrence of this disorder in any domestic species was reported by Angelos et al. (1995), in Charolais cattle.

OMIA ID: 1139Inheritance: As reported by Angelos et al. (1995), six calves from a single Charolais herd...Characterised: YesYear: 1996

Haemophilia A

Khalaj et al. (2009): "A nucleotide substitution of T to A resulting in an amino acid substitution of leucine to histidine (p.Leu2153His) was identified in a highly conserved residue in the C1 domain of factor VIII. Genotyping of 254 normal animals including the pedigree of the affected animals and randomly sampled animals of different breeds confirmed that the substitution is the causative mutation of cattle haemophilia A." Analysis of whole-...

OMIA ID: 437Inheritance: 18Characterised: YesYear: 2009

Syndactyly — Mule foot disease; mulefoot; Haplotype HHM

Syndactyly has been reported in many breeds of cattle in many countries. Most of the documentation, however, concerns its occurrence in US Holsteins, where, as a result of the siring of more than 60,000 calves by a bull who was subsequently shown to be a carrier, the disorder attracted considerable attention (Anon., 1967). The possibility that artificial selection favouring heterozygotes may have contributed to the unacceptably high frequency ...

OMIA ID: 963Inheritance: 5Characterised: YesYear: 2006