Distichiasis
Symptom Information:
Symptom ID: | HPO:0009743 | |||||||||
Synonyms: |
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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 integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of the eyelashes(HPO:0000499) Multiple rows of eyelashes(HPO:0008496) Distichiasis(HPO:0009743) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyelid(HPO:0000492) Abnormality of the eyelashes(HPO:0000499) Multiple rows of eyelashes(HPO:0008496) Distichiasis(HPO:0009743) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) Abnormality of the eyelashes(HPO:0000499) Multiple rows of eyelashes(HPO:0008496) Distichiasis(HPO:0009743) MedDRA: Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Lid, lash and lacrimal structural disorders(MedDRA:10024446) Distichiasis(HPO:0009743) |
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Database Frequency: | 9 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERALVASCULATURE | (OMIM:126320) |
Isolated distichiasis | (Orphanet:99177) |
Lymphedema - distichiasis | (Orphanet:33001) |
Mitochondrial myopathy and sideroblastic anemia | (Orphanet:2598) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Short tarsus - absence of lower eyelashes | (Orphanet:2832) |