Poland syndrome
Human disease
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Poland syndrome
Summary
Poland syndrome is a developmental defect during embryogenesis[1]. It ranks in the top 4% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (1,131 views/month).[2]
Key Facts
- Poland syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Poland syndrome's instance of is recorded as class of disease[4].
- Alfred Poland is named after Poland syndrome[5].
- Poland syndrome is a type of congenital disorder[6].
- Poland syndrome is a type of syndromic breast hypoplasia/aplasia[7].
- Poland syndrome is a type of rare genetic gynecological and obstetrical diseases[8].
- Poland syndrome is a type of syndrome with brachydactyly[9].
- Poland syndrome is a type of disease[10].
- Poland syndrome's Commons category is recorded as Poland syndrome[11].
- Poland syndrome's ICD-9-CM is recorded as 756.89[12].
- Poland syndrome's NCI Thesaurus ID is recorded as C85017[13].
- Poland syndrome's health specialty is recorded as medical genetics[14].
- Poland syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12961[15].
- Poland syndrome's exact match is recorded as http://identifiers.org/doid/DOID:12961[16].
- Poland syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2911[17].
- Poland syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
Poland syndrome ranks in the top 4% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (1,131 views/month).[2] It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[19] It is known by 13 alternative names across languages and contexts.[20]