Search Phenotypes

Interdigital hyperplasia — Bovine interdigital hyperplasia

Zhang et al. (2019): "Normally IH begins with a small and painless protrusion of the interdigital skin which sometimes can already be diagnosed at calf age. In the final stage clinical signs of IH are firm tumor like masses found in the interdigital space with skin lesions that can result in deep necrosis and phlegmonous inflammations."

OMIA ID: 2223Inheritance: This disorder is multifactorial. As summarised by Zhang et al. (2019), "Bovin...Characterised: YesYear: 2019

Interdigital tissue pachydermia

No summary available.

OMIA ID: 563Inheritance: N/ACharacterised: NoYear: N/A

Intervertebral disc disease

No summary available.

OMIA ID: 157Inheritance: N/ACharacterised: NoYear: N/A

Intussusception, susceptibility to

No summary available.

OMIA ID: 1227Inheritance: N/ACharacterised: NoYear: N/A

Iridal hypopigmentation, bilateral

Hollman et al. (2017): "Summarizing the clinical analysis of the examined animals, a bilateral hypopigmentation caused by a hitherto unknown genetic variation strictly affecting iridal coloration was suspected. As the affected animals did not show any other anomalies, syndromes like Chediak-Higashi or Tietz were excluded."

OMIA ID: 2102Inheritance: 5Characterised: NoYear: N/A

Johne's disease, resistance/susceptibility to

No summary available.

OMIA ID: 1905Inheritance: 10Characterised: NoYear: N/A

Joint laxity and dwarfism, congenital

No summary available.

OMIA ID: 570Inheritance: N/ACharacterised: NoYear: N/A

Ketosis, susceptibility to

No summary available.

OMIA ID: 1125Inheritance: 10Characterised: NoYear: N/A

Knobbed acrosome

No summary available.

OMIA ID: 576Inheritance: N/ACharacterised: NoYear: N/A

Lacrimal fistula (redundant)

Merged with OMIA:002852-9913 : Nasolacrimal duct obstruction in Bos taurus (taurine cattle) [06.05.2024].

OMIA ID: 1693Inheritance: N/ACharacterised: NoYear: N/A

Lactoferrin variation

No summary available.

OMIA ID: 2613Inheritance: N/ACharacterised: NoYear: N/A

Lactoglobulin, beta

This phene includes references to studies involving gene edited or genetically modified organisms (GMO). PAEP is the HGNC approved gene symbol for beta-lactglobulin (BLG).

OMIA ID: 2670Inheritance: N/ACharacterised: NoYear: N/A

Lactoglobulin, beta, aberrant low expression

Braunschweig and Leeb (2006) showed that a "C to A transversion at position 215 bp upstream of the translation initiation site" of the beta-lactoglobulin (LBG) gene segregates with aberrant low expression of beta-lactoglobulin. Other symbols for this gene are BLG and PAEP, the latter being the official NCBI symbol.

OMIA ID: 1437Inheritance: 1Characterised: YesYear: 2006

Lameness

No summary available.

OMIA ID: 579Inheritance: 10Characterised: NoYear: N/A

Laminitis

No summary available.

OMIA ID: 1225Inheritance: N/ACharacterised: NoYear: N/A