Pierpont syndrome
human disease
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Pierpont syndrome
Summary
Pierpont syndrome is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Pierpont syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Pierpont syndrome's instance of is recorded as rare disease[4].
- Pierpont syndrome's instance of is recorded as class of disease[5].
- Pierpont syndrome is a type of genetic syndromic intellectual disability[6].
- Pierpont syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- Pierpont syndrome is a type of genetic disease[8].
- Pierpont syndrome is a type of subcutaneous tissue disease[9].
- Pierpont syndrome's genetic association is recorded as TBL1XR1[10].
- Pierpont syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_487825[11].
Why It Matters
Pierpont syndrome is known by 5 alternative names across languages and contexts.[2]