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Trichorhinophalangeal syndrome type 1 (medical condition): A rare genetic disorder characterized by bulbous...more »
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Trichorhinophalangeal syndrome type 1:
»Introduction: Trichorhinophalangeal syndrome type 1
»Symptoms of Trichorhinophalangeal syndrome type 1
Trichorhinophalangeal syndrome type 1: Cone-shaped epiphyses, sparse hypopigmented hair, bulbous nose, variable growth retardation, and occasional mental retardation.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Trichorhinophalangeal syndrome type 1:
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Trichorhinophalangeal syndrome type 1 as a "rare disease".
Source - Orphanet
Trichorhinophalangeal syndrome type 1 (medical condition): See Trichorhinophalangeal syndrome type 1 (disease information).
»Introduction: Trichorhinophalangeal syndrome type 1
»Symptoms of Trichorhinophalangeal syndrome type 1
Trichorhinophalangeal syndrome type 1: Trichorhinophalangeal syndrome type 1 is listed as a type of (or associated with) the following medical conditions in our database:
These medical disease topics may be related to Trichorhinophalangeal syndrome type 1:
Source: Diseases Database
Source: Diseases Database
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