Talk:Tyrosinemia type II

	Medicine portal This article is within the scope of WikiProject Medicine, which recommends that medicine-related articles follow the Manual of Style for medicine-related articles and that biomedical information in any article use high-quality medical sources. Please visit the project page for details or ask questions at Wikipedia talk:WikiProject Medicine.MedicineWikipedia:WikiProject MedicineTemplate:WikiProject Medicinemedicine articles
Mid	This article has been rated as Mid-importance on the project's importance scale.
	This article is supported by the Dermatology task force.

Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Tyrosinemia type II.

PubMed provides review articles from the past five years (limit to free review articles)
The TRIP database provides clinical publications about evidence-based medicine.
Other potential sources include: Centre for Reviews and Dissemination and CDC

It is requested that a photograph be included in this article to improve its quality.
The external tool WordPress Openverse may be able to locate suitable images on Flickr and other web sites.

Upload

Article categorization

This article was initially categorized based on scheme outlined at WP:DERM:CAT. kilbad (talk) 19:52, 12 February 2009 (UTC)[reply]

@Doc James: Hi Dr. I changed the manner of inheritance because many resources states it as autosomal recessive. What do you think? Regards--Avicenno (talk) 20:23, 23 August 2019 (UTC)[reply]

User:Avicenno agree per https://rarediseases.info.nih.gov/diseases/3105/tyrosinemia-type-2 Doc James (talk · contribs · email) 04:38, 24 August 2019 (UTC)[reply]

@Doc James: Hi. I mean for Hanhart syndrome but the talk page redirected me here. --Avicenno (talk) 06:52, 24 August 2019 (UTC)[reply]

Fixed the redirect Doc James (talk · contribs · email) 08:21, 24 August 2019 (UTC)[reply]

Cause of Hanhart is unknown, may be autosomal recessive. Doc James (talk · contribs · email) 08:23, 24 August 2019 (UTC)[reply]