Wt limb-blood syndrome

Preferred Label : Wt limb-blood syndrome;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Neoplasia : Leukemia;

Laboratory abnormalities : No chromosome breakage;

Prefixed ID : %194350;

Details

Origin ID

194350;

UMLS CUI

C1327917;

Automatic exact mappings (from CISMeF team)
- WT limb-blood syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- WT limb blood syndrome [MeSH concept]
- WT limb blood syndrome [MeSH Supplementary Concept]
- WT limb blood syndrome (disorder) [SNOMED CT concept]
- WT limb-blood syndrome [ORDO Disease]
HPO term(s)
- Absent thumb [HPO term]
- Autosomal dominant inheritance [HPO term]
- Clinodactyly of the 5th finger [HPO term]
- Cryptorchidism [HPO term]
- Hypoplastic anemia [HPO term]
- Irregular hyperpigmentation [HPO term]
- Joint contracture of the 5th finger [HPO term]
- Leukemia [HPO term]
- Micrognathia [HPO term]
- Pancytopenia [HPO term]
- Radioulnar synostosis [HPO term]
- Retrognathia [HPO term]
- Sensorineural hearing impairment [HPO term]
- Short phalanx of finger [HPO term]
- Short thumb [HPO term]
- Thrombocytopenia [HPO term]
- Ulnar deviation of the 3rd finger [HPO term]
- Ulnar deviation of thumb [HPO term]
Not associated HPO term(s)
- Abnormality of chromosome stability [HPO term]
- Chromosome breakage [HPO term]
ORDO concept(s)
- WT limb-blood syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- WT limb blood syndrome [MeSH Supplementary Concept]
- WT limb blood syndrome [MeSH concept]
- WT limb blood syndrome (disorder) [SNOMED CT concept]
- WT limb-blood syndrome [ORDO Disease]

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