Prominent eyelashes
Symptom Information:
Symptom ID: | HPO:0011231 | |||||||||
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) Prominent eyelashes(HPO:0011231) 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) Prominent eyelashes(HPO:0011231) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) Abnormality of the eyelashes(HPO:0000499) Prominent eyelashes(HPO:0011231) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Hypertrichoses(MedDRA:10020863) Prominent eyelashes(HPO:0011231) |
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Database Frequency: | 9 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
2p21 microdeletion syndrome | (Orphanet:163693) |
Amaurosis - hypertrichosis | (Orphanet:1021) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Roifman syndrome | (Orphanet:353298) |
Wiedemann-Steiner syndrome | (Orphanet:319182) |