Jawad syndrome
human disease
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Jawad syndrome
Summary
Jawad syndrome is a developmental defect during embryogenesis[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- Jawad syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Jawad syndrome's instance of is recorded as rare disease[4].
- Jawad syndrome's instance of is recorded as class of disease[5].
- Jawad syndrome is a type of syndrome with microcephaly as major feature[6].
- Jawad syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- Jawad syndrome's genetic association is recorded as RBBP8[8].
- Jawad syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_313795[9].
Why It Matters
Jawad syndrome is known by 6 alternative names across languages and contexts.[2]