hanhart's syndrome

Preferred Label : hanhart's syndrome;

Origin ID

D4-01237;

UMLS CUI

C0595985;

Automatic exact mappings (from CISMeF team)
- Aglossia-adactyly syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hanhart syndrome [PASCAL descriptor]
- Hanhart syndrome [MeSH concept]
- Hanhart's syndrome (disorder) [SNOMED CT concept]
- Hypoglossia-hypodactylia [OMIM Phenotype]
- Hypoglossia-hypodactyly syndrome [ORDO Disease]
- hanhart syndrome [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Other congenital malformation syndromes with other skeletal changes [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Branchial arch or oral-acral syndrome [ORDO Disease]
- Genetic branchial arch or oral-acral syndrome [ORDO Disease]
- Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome [ORDO Disease]
- Non-syndromic limb reduction defect [ORDO Disease]
- Oromandibular-limb hypogenesis syndrome [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Hanhart's syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aglossia-adactyly syndrome (disorder) [SNOMED CT concept]
- Hanhart syndrome [MeSH concept]
- Hanhart syndrome [PASCAL descriptor]
- Hanhart's syndrome (disorder) [SNOMED CT concept]
- hanhart syndrome [MeSH Supplementary Concept]