Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0016606> ?p ?o ?g. }
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- MONDO_0016606 IAO_0000115 "OBSOLETE. Prenatal benign hypophosphatasia (PB-HPP) is a very rare form of hypophosphatasia characterized by prenatal skeletal manifestations (limb shortening and bowing) that slowly resolve spontaneously and later develop into the milder infantile, childhood or adult forms of the disease." @default.
- MONDO_0016606 IAO_0000231 OMO_0001000 @default.
- MONDO_0016606 IAO_0000233 "https://github.com/monarch-initiative/mondo/issues/2906" @default.
- MONDO_0016606 normalizedInformationContent "100" @default.
- MONDO_0016606 referenceCount "1" @default.
- MONDO_0016606 consider "MONDO:0600009" @default.
- MONDO_0016606 consider "MONDO:0600010" @default.
- MONDO_0016606 consider "MONDO:0600011" @default.
- MONDO_0016606 hasDbXref "GARD:20662" @default.
- MONDO_0016606 hasDbXref "ICD10CM:E83.3" @default.
- MONDO_0016606 hasDbXref "Orphanet:247638" @default.
- MONDO_0016606 hasDbXref "UMLS:CN201801" @default.
- MONDO_0016606 hasExactSynonym "prenatal benign Rathburn disease" @default.
- MONDO_0016606 hasExactSynonym "prenatal benign phosphoethanolaminuria" @default.
- MONDO_0016606 id "MONDO:0016606" @default.
- MONDO_0016606 inSubset gard_rare @default.
- MONDO_0016606 inSubset nord_rare @default.
- MONDO_0016606 inSubset ordo_clinical_subtype @default.
- MONDO_0016606 inSubset rare @default.
- MONDO_0016606 type Class @default.
- MONDO_0016606 isDefinedBy mondo.owl @default.
- MONDO_0016606 label "obsolete prenatal benign hypophosphatasia" @default.
- MONDO_0016606 subClassOf MONDO_0016606 @default.
- MONDO_0016606 subClassOf Thing @default.
- MONDO_0016606 deprecated "true" @default.
- MONDO_0016606 exactMatch CN201801 @default.
- MONDO_0016606 exactMatch Orphanet_247638 @default.