absence of fingerprints-congenital milia syndrome
0 sources
absence of fingerprints-congenital milia syndrome
Summary
absence of fingerprints-congenital milia syndrome is a hereditary disorder[1]. It draws 24 Wikipedia views per month (hereditary_disorder category, ranking #14 of 25).[2]
Key Facts
- absence of fingerprints-congenital milia syndrome's instance of is recorded as hereditary disorder[3].
- absence of fingerprints-congenital milia syndrome's instance of is recorded as rare disease[4].
- absence of fingerprints-congenital milia syndrome's instance of is recorded as class of disease[5].
- absence of fingerprints-congenital milia syndrome is a type of adermatoglyphia[6].
- absence of fingerprints-congenital milia syndrome is a type of miliaria[7].
- absence of fingerprints-congenital milia syndrome is a type of other genetic epidermal disease[8].
- absence of fingerprints-congenital milia syndrome is a type of other epidermal disorder[9].
- absence of fingerprints-congenital milia syndrome is a type of ectodermal dysplasia[10].
- absence of fingerprints-congenital milia syndrome's genetic association is recorded as SMARCAD1[11].
- absence of fingerprints-congenital milia syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1235[12].
- absence of fingerprints-congenital milia syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1658[13].
- absence of fingerprints-congenital milia syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080725[14].
- absence of fingerprints-congenital milia syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080725[15].
Why It Matters
absence of fingerprints-congenital milia syndrome draws 24 Wikipedia views per month (hereditary_disorder category, ranking #14 of 25).[2]