Vitamin A deficiency

Symptom Information:

Symptom ID: HPO:0004905
Synonyms:
Vitamin A deficiency (disorder) [Orphanet:49620]
Vitamin A Deficiency [Orphanet:49620]
Vitamin A deficiency [OMIM:Vitamin A deficiency]
Vitamin A deficiency [Orphanet:49620]
Vitamin A deficiency [MedDRA:10047586]
Other manifestations of vitamin A deficiency [MedDRA:10047586]
Retinol deficiency [MedDRA:10047586]
Unspecified vitamin A deficiency [MedDRA:10047586]
Quality:
Cross references:
Orphanet:49620 "Vitamin A deficiency" [Orphanet:49620]
OMIM: "Vitamin A deficiency" [OMIM:Vitamin A deficiency]
UMLS:C0042842 "Vitamin A Deficiency" [Orphanet:49620]
Is a (Direct Parents):
HPO         Abnormality of vitamin A metabolism
Orphanet Abnormality of vitamin metabolism
MedDRA Fat soluble vitamin deficiencies and disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of vitamin metabolism(HPO:0100508)
             Abnormality of vitamin A metabolism(HPO:0008372)
                Vitamin A deficiency(HPO:0004905)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Vitamin related disorders(MedDRA:10047635)
       Fat soluble vitamin deficiencies and disorders(MedDRA:10016250)
          Vitamin A deficiency(HPO:0004905)
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Dent disease type 1 (Orphanet:93622)
HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:277350)
Hereditary hypercarotenemia and vitamin A deficiency (Orphanet:199285)