Trimethylaminuria (Support Group) - 476 Members
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Conditions (59):
Trimethylaminuria, Genetic and Rare Conditions, Halitosis, and 56 others
Trimethylaminuria, Genetic and Rare Conditions, Halitosis, Diseases and Conditions, Achalasia, Dercum's Disease, Addison's Disease, Hirschsprung's Disease, Agenesis of Corpus Callosum, Fragile X Syndrome, Anencephaly, PANDA Syndrome, Dandy Walker Syndrome, Cleidocranial Dysplasia, Androgen Insensitivity Syndrome, Pachygyria, Behcet's Syndrome, Marfan syndrome, 1p36 Deletion Syndrome, Cri-du-Chat Syndrome, Darier's Disease, Menkes Kinky Hair Syndrome, Post-Polio Syndrome, Factor V Leiden, Angelman syndrome, Kartagener Syndrome, Fructose Intolerance, Williams Syndrome, Simpson-Golabi-Behmel Syndrome, Inflammatory Linear Verrucous Epidermal Nevus, Acute Intermittent Porphyria, Aarskog Syndrome, Legg-Calve-Perthes Disease, Adrenal Insufficiency, Epidermal Nevus, Complete Androgen Insensitivity Syndrome, Hydrocephalus, Cushings Syndrome, Lissencephaly, Cystic Fibrosis, Adie Syndrome, Cerebral Palsy, Autism / Autism Spectrum, Asperger's Syndrome, Sjogren's Syndrome, Hashimoto's Encephalopathy, Friedreich's Ataxia, Evan's Syndrome, Gulf War syndrome, Huntington's disease, Joubert syndrome, Hailey-Hailey disease, Acromegaly, Langerhans Cell Histiocytosis, Noonan syndrome, Klinefelter's Syndrome, Keratosis Follicularis Squamosa, Brown-Sequard syndrome, Beal's syndrome [hide]
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Groups (26):
Dercum's Disease, Achalasia, Lupus, and 23 others
Dercum's Disease, Achalasia, Lupus, Rare 'Orphan' Disorders, Addison's Disease, Hirschsprung's Disease, Agenesis of Corpus Callosum, Blepharophimosis, PANDAS Syndrome, Anencephaly, Fragile X Syndrome, Dandy Walker Syndrome, Pachygyria, Cleidocranial Dysplasia, Androgen Insensitivity Syndrome, Cushing's Syndrome, Menkes Kinky Hair Syndrome, Microphthalmia, Multiple Endocrine Neoplasia Type 1, Behcet's Syndrome, Beckers Nevus, Hidradenitis Suppurativa, Raynaud's Disease and Phenomenon, Factor V Leiden, Cri-du-Chat Syndrome, Diabetes Insipidus [hide]
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Symptoms (11):
bromhyrosis, Characteristics of ATR-X, Blepharophimosis, and 8 others
bromhyrosis, Characteristics of ATR-X, Blepharophimosis, Sweet Syndrome, Von Willebrand disease, Club Foot, Scleroderma, pyoderma gangrenosum, Castleman's Disease, Symptoms and Side Effects, Tetralogy of Fallot [hide]
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Treatments (5):
Choline-Restricted Diet, Chlorophyllin, trimethylaminuria, and 2 others
Choline-Restricted Diet, Chlorophyllin, trimethylaminuria, Treatments, Tests [hide]
About Trimethylaminuria
The Trimethylaminuria community is a place to find support and information from others living with Trimethylaminuria.
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