Tricho–rhino–phalangeal syndrome
human disease
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Tricho–rhino–phalangeal syndrome
Summary
Tricho–rhino–phalangeal syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Tricho–rhino–phalangeal syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Tricho–rhino–phalangeal syndrome's instance of is recorded as rare disease[3].
- Tricho–rhino–phalangeal syndrome's instance of is recorded as class of disease[4].
- Tricho–rhino–phalangeal syndrome is a type of acromelic dysplasia[5].
- Tricho–rhino–phalangeal syndrome's ICD-9-CM is recorded as 759.89[6].
- Tricho–rhino–phalangeal syndrome's genetic association is recorded as TRPS1[7].
- Tricho–rhino–phalangeal syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_324764[8].