Lacrimation abnormality

Symptom Information:

Symptom ID: HPO:0000632
Abnormality of tear production [HPO:0000632]
Defect of lacrimal system [Orphanet:7850]
Defect/anomaly of lacrimal system [Orphanet:7850]
Cross references:
Orphanet:7850 "Defect/anomaly of lacrimal system" [Orphanet:7850]
Is a (Direct Parents):
HPO         Abnormal eye physiology
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Lacrimation abnormality(HPO:0000632)
Database Frequency: 42 / 7739

All diseases associated with this symptom:

Acrocraniofacial dysostosis (Orphanet:949)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
BOR syndrome (Orphanet:107)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Blepharophimosis - epicanthus inversus - ptosis (Orphanet:126)
Blepharophimosis-intellectual deficit syndrome, SBBYS type (Orphanet:3047)
Branchio-oculo-facial syndrome (Orphanet:1297)
Branchio-otic syndrome (Orphanet:52429)
CHARGE syndrome (Orphanet:138)
Coffin-Siris syndrome (Orphanet:1465)
Contractures - ectodermal dysplasia - cleft lip/palate (Orphanet:1484)
Corneal anesthesia - deafness - intellectual deficit (Orphanet:1051)
Craniofacial-deafness-hand syndrome (Orphanet:1529)
Craniosynostosis - fibular aplasia (Orphanet:1533)
Dacryocystitis - osteopoikilosis (Orphanet:1562)
Deafness - epiphyseal dysplasia - short stature (Orphanet:3218)
Dystrophic epidermolysis bullosa (Orphanet:303)
EEC syndrome (Orphanet:1896)
Facial ectodermal dysplasia (Orphanet:1807)
Fraser syndrome (Orphanet:2052)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Johanson-Blizzard syndrome (Orphanet:2315)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Microtia - eye coloboma - imperforation of the nasolacrimal duct (Orphanet:139450)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Oculocerebrorenal syndrome (Orphanet:534)
Oculotrichoanal syndrome (Orphanet:2717)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
Paroxysmal extreme pain disorder (Orphanet:46348)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Ptosis - upper ocular movement limitation - absence of lacrimal punctum (Orphanet:228396)
Renal-genital-middle ear anomalies (Orphanet:1092)
Rubinstein-Taybi syndrome (Orphanet:783)
Stüve-Wiedemann syndrome (Orphanet:3206)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Williams syndrome (Orphanet:904)