Temple-Baraitser syndrome
medical condition
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Temple-Baraitser syndrome
Summary
Temple-Baraitser syndrome is a developmental defect during embryogenesis[1]. It draws 8 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- Temple-Baraitser syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Temple-Baraitser syndrome's instance of is recorded as rare disease[4].
- Temple-Baraitser syndrome's instance of is recorded as class of disease[5].
- Temple-Baraitser syndrome is a type of syndromic nail anomaly[6].
- Temple-Baraitser syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- Temple-Baraitser syndrome is a type of genetic syndromic intellectual disability[8].
- Temple-Baraitser syndrome's genetic association is recorded as KCNH1[9].
- Temple-Baraitser syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_420561[10].
Why It Matters
Temple-Baraitser syndrome draws 8 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]