Aagenaes syndrome
syndrome that is characterized by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts
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Aagenaes syndrome
Summary
Aagenaes syndrome is a class of disease[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Aagenaes syndrome's instance of is recorded as class of disease[3].
- Aagenaes syndrome is a type of syndrome[4].
- Aagenaes syndrome is a type of primary lymphedema with associated anomalies[5].
- Aagenaes syndrome is a type of genetic vascular anomaly[6].
- Aagenaes syndrome is a type of rare genetic hepatic disease[7].
- Aagenaes syndrome is a type of syndromic lymphedema[8].
- Aagenaes syndrome is a type of rare genetic immune disease[9].
- Aagenaes syndrome is a type of disease[10].
- Aagenaes syndrome's Commons category is recorded as Aagenaes syndrome[11].
- Aagenaes syndrome's symptoms and signs is recorded as hepatitis[12].
- Aagenaes syndrome's ICD-9-CM is recorded as 576.8[13].
- Aagenaes syndrome's NCI Thesaurus ID is recorded as C35709[14].
- Aagenaes syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_6691[15].
- Aagenaes syndrome's exact match is recorded as http://identifiers.org/doid/DOID:6691[16].
- Aagenaes syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- Aagenaes syndrome's has phenotype is recorded as liver cirrhosis[18].
- Aagenaes syndrome's has phenotype is recorded as cholestasis[19].
Why It Matters
Aagenaes syndrome has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 21 alternative names across languages and contexts.[20]