"adermatoglyphia" meaning in English

See adermatoglyphia in All languages combined, or Wiktionary

Noun

IPA: /eɪˌdɜː.mə.təʊˈɡlɪ.fɪ.ə/ [Received-Pronunciation], /eɪˌdɝ.mə.təˈɡlɪ.fi.ə/ [General-American] Audio: LL-Q1860 (eng)-Vealhurl-adermatoglyphia.wav
enPR: ādûr'mətōglĭʹfĭə [Received-Pronunciation] Etymology: From Ancient Greek ἀ- (a-, the alpha privativum, a prefix forming words having a sense opposite to the word or stem to which it is attached; a-) + δέρμα (dérma, “skin”) + γλυφή (gluphḗ, “carving”) + -ία (-ía, suffix forming feminine abstract nouns); analysable as a- + dermato- + glyph + -a. Etymology templates: {{root|en|ine-pro|*glewbʰ-}}, {{der|en|grc|ἀ-|pos=the alpha privativum, a prefix forming words having a sense opposite to the word or stem to which it is attached; a-}} Ancient Greek ἀ- (a-, the alpha privativum, a prefix forming words having a sense opposite to the word or stem to which it is attached; a-), {{affix|en|a-|dermato-|glyph|-a}} a- + dermato- + glyph + -a Head templates: {{en-noun|-}} adermatoglyphia (uncountable)
  1. The rare congenital absence of epidermal ridges (fingerprints and toeprints). Tags: uncountable
    Sense id: en-adermatoglyphia-en-noun-RUV-Q95T
  2. The autosomally dominant genetic disorder which causes this condition. Tags: uncountable Categories (topical): Fingers, Genetic disorders Translations (rare congenital absence of epidermal ridges; genetic disorder which causes this condition): 皮纹病 (Chinese Mandarin), adermatoglifia [feminine] (Galician), Adermatoglyphie (German), αδερματογλυφία (adermatoglyfía) (Greek), adermatoglifia (Indonesian), adermatoglifia (Italian), адерматоглифия (adermatoglifiä) (Kazakh), adermatoglifia (Portuguese), adermatoglifia (Spanish)
    Sense id: en-adermatoglyphia-en-noun-6~XjpyR7 Disambiguation of Fingers: 44 56 Disambiguation of Genetic disorders: 11 89 Categories (other): English entries with incorrect language header, English terms prefixed with a-, English terms prefixed with dermato-, English terms suffixed with -a, Entries with translation boxes, Pages with 1 entry, Pages with entries, Terms with Galician translations, Terms with German translations, Terms with Greek translations, Terms with Indonesian translations, Terms with Italian translations, Terms with Kazakh translations, Terms with Mandarin translations, Terms with Portuguese translations, Terms with Spanish translations Disambiguation of English entries with incorrect language header: 21 79 Disambiguation of English terms prefixed with a-: 44 56 Disambiguation of English terms prefixed with dermato-: 44 56 Disambiguation of English terms suffixed with -a: 29 71 Disambiguation of Entries with translation boxes: 23 77 Disambiguation of Pages with 1 entry: 20 80 Disambiguation of Pages with entries: 20 80 Disambiguation of Terms with Galician translations: 24 76 Disambiguation of Terms with German translations: 26 74 Disambiguation of Terms with Greek translations: 26 74 Disambiguation of Terms with Indonesian translations: 24 76 Disambiguation of Terms with Italian translations: 24 76 Disambiguation of Terms with Kazakh translations: 24 76 Disambiguation of Terms with Mandarin translations: 24 76 Disambiguation of Terms with Portuguese translations: 29 71 Disambiguation of Terms with Spanish translations: 23 77 Disambiguation of 'rare congenital absence of epidermal ridges; genetic disorder which causes this condition': 41 59
The following are not (yet) sense-disambiguated
Derived forms: adermatoglyphic Related terms: dermatoglyphic, dermatoglyphics
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          "text": "Dyskeratosis congenita is a rare congenital syndrome, characterized by the triad of reticular skin pigmentation, mucosal leukoplakia, and nail dystrophy, plus the predisposition to bone marrow failure and malignancy. […] Other cutaneous findings may include alopecia, hyperkeratosis of the palms and soles, and adermatoglyphia (loss of dermal ridges on fingers and toes).",
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          "text": "A problem in forensics for this type of identification is people who are born without or do not have fingerprints. A Swiss woman and a portion of her family members were born without fingerprints in a condition called adermatoglyphia. Her genotype was mapped and discovered she had a point mutation in the SMARCAD1 gene located in the chromosome 4q22, which caused her to be born without the loops, whorls, and arches in her digits that are associated with fingerprints[…]. There are other cases that result in adermatoglyphia such as the disease dermatopathia pigmentosa reticularis, Naegeli syndrome, and manual removal of one's fingerprints which is a temporary but painful technique.",
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          "_dis1": "41 59",
          "code": "cmn",
          "lang": "Chinese Mandarin",
          "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
          "word": "皮纹病"
        },
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          "_dis1": "41 59",
          "code": "gl",
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          "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
          "tags": [
            "feminine"
          ],
          "word": "adermatoglifia"
        },
        {
          "_dis1": "41 59",
          "code": "de",
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          "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
          "word": "Adermatoglyphie"
        },
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          "code": "el",
          "lang": "Greek",
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          "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
          "word": "αδερματογλυφία"
        },
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          "_dis1": "41 59",
          "code": "id",
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          "word": "adermatoglifia"
        },
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          "word": "адерматоглифия"
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          "_dis1": "41 59",
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          "word": "adermatoglifia"
        },
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          "_dis1": "41 59",
          "code": "es",
          "lang": "Spanish",
          "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
          "word": "adermatoglifia"
        }
      ]
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          "text": "A problem in forensics for this type of identification is people who are born without or do not have fingerprints. A Swiss woman and a portion of her family members were born without fingerprints in a condition called adermatoglyphia. Her genotype was mapped and discovered she had a point mutation in the SMARCAD1 gene located in the chromosome 4q22, which caused her to be born without the loops, whorls, and arches in her digits that are associated with fingerprints[…]. There are other cases that result in adermatoglyphia such as the disease dermatopathia pigmentosa reticularis, Naegeli syndrome, and manual removal of one's fingerprints which is a temporary but painful technique.",
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    {
      "code": "cmn",
      "lang": "Chinese Mandarin",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "皮纹病"
    },
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      "code": "gl",
      "lang": "Galician",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "tags": [
        "feminine"
      ],
      "word": "adermatoglifia"
    },
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      "code": "de",
      "lang": "German",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "Adermatoglyphie"
    },
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      "code": "el",
      "lang": "Greek",
      "roman": "adermatoglyfía",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "αδερματογλυφία"
    },
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      "code": "id",
      "lang": "Indonesian",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "adermatoglifia"
    },
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      "code": "it",
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      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "adermatoglifia"
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      "code": "kk",
      "lang": "Kazakh",
      "roman": "adermatoglifiä",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "адерматоглифия"
    },
    {
      "code": "pt",
      "lang": "Portuguese",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "adermatoglifia"
    },
    {
      "code": "es",
      "lang": "Spanish",
      "sense": "rare congenital absence of epidermal ridges; genetic disorder which causes this condition",
      "word": "adermatoglifia"
    }
  ],
  "word": "adermatoglyphia"
}

Download raw JSONL data for adermatoglyphia meaning in English (7.4kB)


This page is a part of the kaikki.org machine-readable English dictionary. This dictionary is based on structured data extracted on 2024-12-21 from the enwiktionary dump dated 2024-12-04 using wiktextract (d8cb2f3 and 4e554ae). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.

If you use this data in academic research, please cite Tatu Ylonen: Wiktextract: Wiktionary as Machine-Readable Structured Data, Proceedings of the 13th Conference on Language Resources and Evaluation (LREC), pp. 1317-1325, Marseille, 20-25 June 2022. Linking to the relevant page(s) under https://kaikki.org would also be greatly appreciated.