Alacrima

Symptom Information:

Symptom ID: HPO:0000522
Synonyms:
Alacrima (disorder) [Orphanet:4600]
Alacrima [Orphanet:4600]
Alacrima [OMIM:Alacrima]
Congenital alacrimia [Orphanet:4600]
Alacrima (dry eye syndrome) [OMIM:Alacrima (dry eye syndrome)]
Quality:
Cross references:
Orphanet:4600 "Congenital alacrimia" [Orphanet:4600]
OMIM: "Alacrima" [OMIM:Alacrima]
OMIM: "Alacrima (dry eye syndrome)" [OMIM:Alacrima (dry eye syndrome)]
UMLS:C0344505 "Alacrima" [HPO:0000522]
UMLS:C0344505 "Alacrima" [Orphanet:4600]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Decreased lacrimation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Lacrimation abnormality(HPO:0000632)
                Decreased lacrimation(HPO:0000633)
                   Alacrima(HPO:0000522)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME (OMIM:231550)
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE (OMIM:601549)
Familial dysautonomia (Orphanet:1764)
HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE (OMIM:240000)
Hereditary sensory and autonomic neuropathy type 1B (Orphanet:139564)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Intellectual deficit - alacrima - achalasia (Orphanet:289483)
Isolated congenital alacrima (Orphanet:91416)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
OTOFACIOCERVICAL SYNDROME 2 (OMIM:615560)
Schinzel-Giedion syndrome (Orphanet:798)
Triple A syndrome (Orphanet:869)