Fanconi-like syndrome

Preferred Label : Fanconi-like syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 227850;

Details

Origin ID

227850;

UMLS CUI

C0151638;

Currated CISMeF NLP mapping
- Fanconi like syndrome [MeSH concept]
- Fanconi-like syndrome [DO Concept]
- Fanconi-like syndrome [MedDRA LLT]
- Fanconi-like syndrome (disorder) [SNOMED CT concept]
- Syndrome Fanconi-like [MedDRA LLT]
- fanconi like syndrome [MeSH Supplementary Concept]
DO Cross reference
- Fanconi-like syndrome [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Multiple bilateral pneumothoraces [HPO term]
- Multiple cutaneous malignancies [HPO term]
- Osteomyelitis [HPO term]
- Pancytopenia [HPO term]
- Recurrent lower respiratory tract infections [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fanconi like syndrome [MeSH concept]
- Fanconi-like syndrome [MedDRA LLT]
- Fanconi-like syndrome [DO Concept]
- Fanconi-like syndrome (disorder) [SNOMED CT concept]
- Syndrome Fanconi-like [MedDRA LLT]
- fanconi like syndrome [MeSH Supplementary Concept]

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