Hanhart syndrome
human disease
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Hanhart syndrome
Summary
Hanhart syndrome is a hereditary disorder[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Hanhart syndrome's instance of is recorded as hereditary disorder[3].
- Hanhart syndrome's instance of is recorded as head and neck disease[4].
- Hanhart syndrome's instance of is recorded as developmental defect during embryogenesis[5].
- Hanhart syndrome's instance of is recorded as class of disease[6].
- Hanhart syndrome is a type of hypoglossia[7].
- Hanhart syndrome is a type of Hypodactylia[8].
- Hanhart syndrome is a type of oromandibular-limb hypogenesis syndrome[9].
- Hanhart syndrome is a type of syndrome with limb reduction defects[10].
- Hanhart syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[11].
- Hanhart syndrome is a type of branchial arch or oral-acral syndrome[12].
- Hanhart syndrome's described by source is recorded as Otto's encyclopedia[13].
- Hanhart syndrome's ICD-9-CM is recorded as 759.89[14].
- Hanhart syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_989[15].
Why It Matters
Hanhart syndrome has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 9 alternative names across languages and contexts.[16]