adult hypophosphatasia
hypophosphatasia that has material basis in a heterozygous mutation of ALPL on chromosome 1p36.12
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adult hypophosphatasia
Summary
adult hypophosphatasia is a class of disease[1].
Key Facts
- adult hypophosphatasia's instance of is recorded as class of disease[2].
- adult hypophosphatasia's subclass of is recorded as hypophosphatasia[3].
- adult hypophosphatasia's OMIM ID is recorded as 146300[4].
- adult hypophosphatasia's Disease Ontology ID is recorded as DOID:0110913[5].
- adult hypophosphatasia's Orphanet ID is recorded as 247676[6].
- adult hypophosphatasia's genetic association is recorded as ALPL[7].
- adult hypophosphatasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110913[8].
- adult hypophosphatasia's exact match is recorded as http://identifiers.org/doid/DOID:0110913[9].
- adult hypophosphatasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_247676[10].
- adult hypophosphatasia's UMLS CUI is recorded as C0268413[11].
- adult hypophosphatasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- adult hypophosphatasia's Experimental Factor Ontology ID is recorded as 0021431[13].