causes blue-tinged skin and reduced oxygen delivery because hemoglobin malfunctions.

is a rare disorder causing low oxygen levels and atypical genital development.

is a pattern of birth defects linked to methimazole exposure in pregnancy.

is a rare inherited disorder that causes high methionine levels.

happens when methotrexate builds up and causes harmful side effects.

is an abnormal growth of lymph cells linked to methotrexate use.

is a type of lymphoma-like disorder linked to methotrexate treatment.

is a type of asthma triggered by allergic reactions to methyl isocyanate.

is a rare inherited disorder affecting vitamin B12 processing and body function.

is a rare inherited B12-processing disorder causing homocystinuria, megaloblastic anemia, neurologic symptoms.

is a rare inherited B12-processing disorder causing high homocysteine and anemia.

is a rare inherited disorder affecting how the body processes certain proteins.

is a rare inherited disorder that prevents normal breakdown of certain proteins.

is an inherited disorder affecting vitamin B12 processing, growth, and development.

is a rare inherited disorder affecting vitamin B12 processing and metabolism.

is an inherited disorder affecting vitamin B12 processing and many body systems.

is a rare inherited disorder affecting vitamin B12 processing and metabolism.

is a rare inherited disorder affecting how the body processes protein.

is a rare inherited disorder affecting vitamin B12 processing and brain development.

is a rare inherited disorder that prevents proper breakdown of certain proteins.

is a rare inherited disorder affecting vitamin B12 processing and metabolism.

is a rare inherited disorder affecting vitamin B12 processing and metabolism.

is a rare inherited disorder affecting vitamin B12 processing and metabolism.

is a rare inherited disorder that affects vitamin B12 processing.