Chudley-McCullough syndrome
human disease
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Summary
Chudley-McCullough syndrome is a head and neck disease[1]. It draws 92 Wikipedia views per month (head_and_neck_disease category, ranking #59 of 92).[2]
Key Facts
- Chudley-McCullough syndrome's instance of is recorded as head and neck disease[3].
- Chudley-McCullough syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Chudley-McCullough syndrome's instance of is recorded as rare disease[5].
- Chudley-McCullough syndrome's instance of is recorded as class of disease[6].
- Chudley-McCullough syndrome is a type of genetic deafness[7].
- Chudley-McCullough syndrome is a type of syndromic genetic deafness[8].
- Chudley-McCullough syndrome is a type of other syndrome with a central nervous system malformation as major feature[9].
- Chudley-McCullough syndrome's genetic association is recorded as GPSM2[10].
- Chudley-McCullough syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_314597[11].
Why It Matters
Chudley-McCullough syndrome draws 92 Wikipedia views per month (head_and_neck_disease category, ranking #59 of 92).[2] It is known by 11 alternative names across languages and contexts.[12]