Lacrimation abnormality
Symptom Information:
Symptom ID: | HPO:0000632 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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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) MedDRA: |
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Database Frequency: | 42 / 7739 | |||
Resource: |
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) |