Premature aging syndrome, okamoto type

Preferred Label : Premature aging syndrome, okamoto type;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ? Autosomal recessive;

Prefixed ID : 601811;

Details

Origin ID

601811;

UMLS CUI

C1866183;

Automatic exact mappings (from CISMeF team)
- premature aging, okamoto type [MeSH concept]
Currated CISMeF NLP mapping
- premature aging syndrome, okamoto type [MeSH concept]
- premature aging syndrome, okamoto type [MeSH Supplementary Concept]
- premature aging, okamoto type [MeSH Supplementary Concept]
HPO term(s)
- Abnormal hair morphology [HPO term]
- Abnormality of blood and blood-forming tissues [HPO term]
- Abnormality of the pinna [HPO term]
- Autosomal recessive inheritance [HPO term]
- Cataract [HPO term]
- Depressed nasal bridge [HPO term]
- Diabetes mellitus [HPO term]
- Flattened nasal bridge [HPO term]
- Growth abnormality [HPO term]
- Low-set ears [HPO term]
- Microcephaly [HPO term]
- Neoplasm [HPO term]
- Osteoporosis [HPO term]
- Osteosarcoma [HPO term]
- Round face [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- premature aging syndrome, okamoto type [MeSH Supplementary Concept]
- premature aging syndrome, okamoto type [MeSH concept]

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