CHILD syndrome
human disease
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CHILD syndrome
Summary
CHILD syndrome is a head and neck disease[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- CHILD syndrome's instance of is recorded as head and neck disease[3].
- CHILD syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- CHILD syndrome's instance of is recorded as rare disease[5].
- CHILD syndrome's instance of is recorded as class of disease[6].
- CHILD syndrome is a type of hereditary eye tumor[7].
- CHILD syndrome is a type of nevus[8].
- CHILD syndrome is a type of benign neoplasm of cornea[9].
- CHILD syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[10].
- CHILD syndrome is a type of malformation syndrome with skin/mucosae involvement[11].
- CHILD syndrome is a type of syndrome[12].
- CHILD syndrome is a type of X-linked dominant disease[13].
- CHILD syndrome's ICD-9-CM is recorded as 759.89[14].
- CHILD syndrome's health specialty is recorded as medical genetics[15].
- CHILD syndrome's genetic association is recorded as NSDHL[16].
- CHILD syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_139[17].
- CHILD syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111822[18].
- CHILD syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111822[19].
Why It Matters
CHILD syndrome has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[20]