Maxillonasal dysplasia, binder type

Preferred Label : Maxillonasal dysplasia, binder type;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Binder syndrome;

Inheritance : Autosomal dominant vs. multifactorial; heterogeneous;

Prefixed ID : %155050;

Details

Origin ID

155050;

UMLS CUI

C0220692;

Automatic exact mappings (from CISMeF team)
- Binder syndrome [DO Concept]
Currated CISMeF NLP mapping
- Binder's syndrome [MedDRA LLT]
- Maxillonasal dysplasia [MedDRA Preferred Term]
- Maxillonasal dysplasia [ICD-11 More detail]
- Maxillonasal dysplasia [PASCAL descriptor]
- Maxillonasal dysplasia [ORDO Disease]
- Maxillonasal dysplasia syndrome (disorder) [SNOMED CT concept]
- Maxillonasal dysplasia, Binder type [MeSH concept]
- maxillonasal dysplasia, binder type [MeSH Supplementary Concept]
DO Cross reference
- Binder syndrome [DO Concept]
HPO term(s)
- Dental malocclusion [HPO term]
- Depressed nasal bridge [HPO term]
- Flattened nasal bridge [HPO term]
- Heterogeneous [HPO term]
- Large earlobe [HPO term]
- Patchy distortion of vertebrae [HPO term]
- Prominent ear lobes [HPO term]
- Short columella [HPO term]
- Short distal phalanx of finger [HPO term]
- Short nose [HPO term]
- Vertebral clefting [HPO term]
ORDO concept(s)
- Maxillonasal dysplasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Binder syndrome [DO Concept]
- Binder's syndrome [MedDRA LLT]
- Maxillonasal dysplasia [MedDRA Preferred Term]
- Maxillonasal dysplasia [ORDO Disease]
- Maxillonasal dysplasia [PASCAL descriptor]
- Maxillonasal dysplasia [ICD-11 More detail]
- Maxillonasal dysplasia syndrome (disorder) [SNOMED CT concept]
- Maxillonasal dysplasia, Binder type [MeSH concept]
- maxillonasal dysplasia, binder type [MeSH Supplementary Concept]

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