Myhre syndrome
medical condition
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Myhre syndrome
Summary
Myhre syndrome is a hereditary disorder[1]. It draws 50 Wikipedia views per month (hereditary_disorder category, ranking #6 of 25).[2]
Key Facts
- Myhre syndrome's instance of is recorded as hereditary disorder[3].
- Myhre syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Myhre syndrome's instance of is recorded as rare disease[5].
- Myhre syndrome's instance of is recorded as class of disease[6].
- Myhre syndrome is a type of syndromic intellectual disability[7].
- Myhre syndrome is a type of multiple abnormalities[8].
- Myhre syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[9].
- Myhre syndrome is a type of genetic syndromic intellectual disability[10].
- Myhre syndrome's ICD-9-CM is recorded as 759.89[11].
- Myhre syndrome's NCI Thesaurus ID is recorded as C123815[12].
- Myhre syndrome's genetic association is recorded as SMAD4[13].
- Myhre syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2588[14].
Why It Matters
Myhre syndrome draws 50 Wikipedia views per month (hereditary_disorder category, ranking #6 of 25).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[15] It is known by 10 alternative names across languages and contexts.[16]