OMIA:000536-9031 : Hypothyroidism, congenital in Gallus gallus (chicken) |
In other species: rock pigeon , dog , lesser panda , domestic cat , horse , goat , sheep
Categories: Endocrine / exocrine gland phene (incl mammary gland)
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 274500 (trait) , 606765 (gene)
Links to MONDO diseases:
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Deficiency of thyroid gland activity. Also known as Goiterous congenital hypothyroidism; Congenital hypothyroidism; Thyroid dyshormonogenesis. This disorder can be caused by mutations in different genes, and forms of the disease exist that are not inherited.
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000536-9031: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1966 | Cole, R.K. : |
| Hereditary hypothyroidism in the domestic fowl Genetics 53:1021-1033, 1966. Pubmed reference: 5958909. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005