Talk:Tyrosinemia type II

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Article categorization[edit]

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]