Rothmund-Thomson syndrome
human disease
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Rothmund-Thomson syndrome
Summary
Rothmund-Thomson syndrome is a developmental defect during embryogenesis[1]. It draws 169 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #93 of 308).[2]
Key Facts
- Rothmund-Thomson syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Rothmund-Thomson syndrome's instance of is recorded as designated intractable/rare disease[4].
- Rothmund-Thomson syndrome's instance of is recorded as rare disease[5].
- Rothmund-Thomson syndrome's instance of is recorded as class of disease[6].
- August von Rothmund is named after Rothmund-Thomson syndrome[7].
- Rothmund-Thomson syndrome is a type of DNA repair-deficiency disorder[8].
- Rothmund-Thomson syndrome is a type of skin disease[9].
- Rothmund-Thomson syndrome is a type of photodermatosis[10].
- Rothmund-Thomson syndrome is a type of hereditary neoplastic syndromes[11].
- Rothmund-Thomson syndrome is a type of rare genetic developmental defect during embryogenesis[12].
- Rothmund-Thomson syndrome is a type of hereditary poikiloderma[13].
- Rothmund-Thomson syndrome is a type of ectodermal malformation syndrome associated with ocular features[14].
- Rothmund-Thomson syndrome is a type of dentocutaneous disease with cataract[15].
- Rothmund-Thomson syndrome is a type of progeroid syndrome[16].
- Rothmund-Thomson syndrome is a type of genetic photodermatosis[17].
- Rothmund-Thomson syndrome's Commons category is recorded as Rothmund–Thomson syndrome[18].
- Rothmund-Thomson syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4471[19].
- Rothmund-Thomson syndrome's ICD-9-CM is recorded as 759.89[20].
- Rothmund-Thomson syndrome's NCI Thesaurus ID is recorded as C3335[21].
- Rothmund-Thomson syndrome's health specialty is recorded as medical genetics[22].
- Rothmund-Thomson syndrome's genetic association is recorded as RECQL4[23].
- Rothmund-Thomson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2732[24].
- Rothmund-Thomson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:2732[25].
- Rothmund-Thomson syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2909[26].
- Rothmund-Thomson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
Rothmund-Thomson syndrome draws 169 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #93 of 308).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] It is known by 9 alternative names across languages and contexts.[29]