adermatoglyphia
rare genetic disorder causing lack of fingerprints
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adermatoglyphia
Summary
adermatoglyphia is a developmental defect during embryogenesis[1]. adermatoglyphia has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- adermatoglyphia's instance of is recorded as developmental defect during embryogenesis[3].
- adermatoglyphia's instance of is recorded as rare disease[4].
- adermatoglyphia's instance of is recorded as class of disease[5].
- adermatoglyphia is a type of congenital physical abnormality[6].
- adermatoglyphia is a type of malformation syndrome with skin/mucosae involvement[7].
- adermatoglyphia is a type of congenital malformations of the dermatoglyphs[8].
- adermatoglyphia is a type of skin disease[9].
- adermatoglyphia is a type of autosomal dominant disease[10].
- adermatoglyphia is a type of disease[11].
- adermatoglyphia's genetic association is recorded as SMARCAD1[12].
- adermatoglyphia's exact match is recorded as http://purl.obolibrary.org/obo/HP_0007455[13].
- adermatoglyphia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_289465[14].
- adermatoglyphia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111357[15].
- adermatoglyphia's exact match is recorded as http://identifiers.org/doid/DOID:0111357[16].
Why It Matters
adermatoglyphia has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] adermatoglyphia is known by 11 alternative names across languages and contexts.[17]