Meckel syndrome
a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia.
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Meckel syndrome
Summary
Meckel syndrome is a rare disease[1]. It draws 108 Wikipedia views per month (rare_disease category, ranking #197 of 627).[2]
Key Facts
- Meckel syndrome's instance of is recorded as rare disease[3].
- Meckel syndrome's instance of is recorded as class of disease[4].
- Johann Friedrich Meckel the younger is named after Meckel syndrome[5].
- Georg Benno Gruber is named after Meckel syndrome[6].
- Meckel syndrome is a type of ciliopathy[7].
- Meckel syndrome is a type of autosomal recessive[8].
- Meckel syndrome is a type of syndrome[9].
- Meckel syndrome is a type of disease[10].
- Meckel syndrome's Commons category is recorded as Meckel syndrome[11].
- Meckel syndrome's ICD-9-CM is recorded as 753.1[12].
- Meckel syndrome's ICD-9-CM is recorded as 753.10[13].
- Meckel syndrome's NCI Thesaurus ID is recorded as C98978[14].
- Meckel syndrome's health specialty is recorded as medical genetics[15].
- Meckel syndrome's genetic association is recorded as MKS1[16].
- Meckel syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050778[17].
- Meckel syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050778[18].
- Meckel syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_564[19].
- Meckel syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
Meckel syndrome draws 108 Wikipedia views per month (rare_disease category, ranking #197 of 627).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[21] It is known by 20 alternative names across languages and contexts.[22]