Agnathia-holoprosencephaly-situs inversus: A very rare disorder characterized by a small or absent jaw, developmental brain defect and internal organs situated on the wrong side of the body (situs inversus). The severity and range of symptoms is variable. More detailed information about the symptoms, causes, and treatments of Agnathia-holoprosencephaly-situs inversus is available below.
See full list of 25 symptoms of Agnathia-holoprosencephaly-situs inversus
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Agnathia-holoprosencephaly-situs inversus as a "rare disease".
Source - Orphanet
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