infantile hypophosphatasia
hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12
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infantile hypophosphatasia
Summary
infantile hypophosphatasia is a class of disease[1].
Key Facts
- infantile hypophosphatasia's instance of is recorded as class of disease[2].
- infantile hypophosphatasia's subclass of is recorded as hypophosphatasia[3].
- infantile hypophosphatasia's OMIM ID is recorded as 241500[4].
- infantile hypophosphatasia's Disease Ontology ID is recorded as DOID:0110914[5].
- infantile hypophosphatasia's Orphanet ID is recorded as 247651[6].
- infantile hypophosphatasia's genetic association is recorded as ALPL[7].
- infantile hypophosphatasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110914[8].
- infantile hypophosphatasia's exact match is recorded as http://identifiers.org/doid/DOID:0110914[9].
- infantile hypophosphatasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_247651[10].
- infantile hypophosphatasia's UMLS CUI is recorded as C0268412[11].
- infantile hypophosphatasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- infantile hypophosphatasia's UniProt disease ID is recorded as DI-03099[13].
- infantile hypophosphatasia's Experimental Factor Ontology ID is recorded as 0021797[14].