Related Issues (20)
- Inheritance type inconsistencies HOT 3
- ORDO: Autosomal dominant non-syndromic intellectual disability is classified as etiological subtype HOT 3
- ORDO: X-linked nonsyndromic deafness HOT 5
- rhabdoid cancer HOT 1
- potential Legacy_Concept_Name issues from NCIT (Fanconi Anemia vs Syndrome)
- loose classes? HOT 2
- ORDO: Text definitions sometimes truncated HOT 8
- Orphanet disease IDs without classification and not in ORDO HOT 1
- Genetic hypertension is_a renal disease? HOT 1
- ORDO constitutional vs acquired alplastic anemia HOT 1
- familial isolated restrictive cardiomyopathy HOT 1
- Orpha vs Orphanet HOT 5
- Self loop for MONDO:0010765 HOT 2
- Anti-NMDA Receptor Encephalitis HOT 10
- Missing Orphanet Diseases HOT 4
- Retinoblastoma: hereditary or non hereditary HOT 1
- Some disease description text has strange references embedded HOT 1
- Report on metrics since 2016-09-01 HOT 1
- GO import outdated, causing unspecified reasoning behaviour HOT 1
- Move issues from here to new repo, or close them HOT 2
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from monarch-disease-ontology-retired.