Erythrocytosis, familial, 7

Preferred Label : Erythrocytosis, familial, 7;

Symbol : ECYT7;

CISMeF acronym : ECYT7;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Erythrocytosis, alpha-globin type; Polycythemia, alpha-globin type;

Prefixed ID : #617981;

Details

Origin ID

617981;

UMLS CUI

C4693823;

Automatic exact mappings (from CISMeF team)
- HBA1 wt Allele [NCIt concept]
- HBA2 wt Allele [NCIt concept]
- familial erythrocytosis 7 [DO Concept]
DO Cross reference
- familial erythrocytosis 7 [DO Concept]
Genes related to phenotype
- Hemoglobin--alpha locus 1 [OMIM gene]
- Hemoglobin--alpha locus 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Increased hematocrit [HPO term]
- Polycythemia [HPO term]
Not associated HPO term(s)
- Increased hemoglobin [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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