Trichorhinophalangeal syndrome type 3: A rare inherited disorder involving hair, face, teeth, and bone abnormalities. The type and severity of symptoms is variable. More detailed information about the symptoms, causes, and treatments of Trichorhinophalangeal syndrome type 3 is available below.
See full list of 18 symptoms of Trichorhinophalangeal syndrome type 3
Read more about complications of Trichorhinophalangeal syndrome type 3.
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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 Trichorhinophalangeal syndrome type 3 as a "rare disease".
Source - Orphanet
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