Wikidata entity: Q1023604
| P373 | Commons category | String | CHARGE syndrome | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P1325 | external data available at URL | Url | None | ??? |
| P2293 | genetic association | ... | Q15311448 (CHD7) | CHD7 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1692 | ICD-9-CM | String | 759.89 | ??? |
| P667 | ICPC 2 ID | String | A90 | ??? |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q112965645 (symptom or sign) | symptom or sign |
| P31 | instance of | ... | Q42303753 (designated intractable/rare disease) | designated intractable/rare disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q55789477 (head and neck disease) | head and neck disease |
| P1748 | NCI Thesaurus ID | String | C75100 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q179630 (syndrome) | syndrome |
| P279 | subclass of | ... | Q55785289 (multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome) | multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome |
| P279 | subclass of | ... | Q55785336 (syndromic developmental defect of the eye) | syndromic developmental defect of the eye |
| P279 | subclass of | ... | Q55785513 (syndrome or malformation associated with head and neck malformations) | syndrome or malformation associated with head and neck malformations |
| P279 | subclass of | ... | Q55785518 (rare syndrome with cardiac malformations) | rare syndrome with cardiac malformations |
| P279 | subclass of | ... | Q55785600 (syndromic urogenital tract malformation) | syndromic urogenital tract malformation |
| P279 | subclass of | ... | Q55785601 (rare abdominal surgical disease) | rare abdominal surgical disease |
| P279 | subclass of | ... | Q55785844 (rare genetic bone disease) | rare genetic bone disease |
| P279 | subclass of | ... | Q55787699 (immunodeficiency due to absence of thymus) | immunodeficiency due to absence of thymus |
| P279 | subclass of | ... | Q55788046 (rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism) | rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism |
| P279 | subclass of | ... | Q55788734 (syndromic genetic deafness) | syndromic genetic deafness |
| P279 | subclass of | ... | Q55788832 (syndromic renal or urinary tract malformation) | syndromic renal or urinary tract malformation |
| P279 | subclass of | ... | Q55789234 (lens shape anomaly) | lens shape anomaly |
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log id: 5267857