Ackerman syndrome

Preferred Label : Ackerman syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Molar roots, pyramidal, with juvenile glaucoma and unusual upper lip; Glaucoma, juvenile, with unusual upper lip and dental roots;

Inheritance : Autosomal recessive;

Prefixed ID : 200970;

Details

Origin ID

200970;

UMLS CUI

C1860167;

Automatic exact mappings (from CISMeF team)
- Ackerman syndrome [ICD-11 More detail]
- Ackerman syndrome (disorder) [SNOMED CT concept]
- Interstitial granulomatous dermatitis with arthritis [ORDO Disease]
Currated CISMeF NLP mapping
- Ackerman syndrome [MeSH concept]
- Pyramidal molars-abnormal upper lip syndrome [ORDO Disease]
- ackerman syndrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Broad philtrum [HPO term]
- Glaucoma [HPO term]
- Taurodontia [HPO term]
ORDO concept(s)
- Pyramidal molars-abnormal upper lip syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ackerman syndrome [MeSH concept]
- Ackerman syndrome (disorder) [SNOMED CT concept]
- Pyramidal molars-abnormal upper lip syndrome [ORDO Disease]
- ackerman syndrome [MeSH Supplementary Concept]

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