Sparse lateral eyebrow
Symptom Information:
Symptom ID: | HPO:0005338 | ||||||||||||
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 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 eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) Sparse and thin eyebrow(HPO:0000535) Sparse lateral eyebrow(HPO:0005338) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) Sparse and thin eyebrow(HPO:0000535) Sparse lateral eyebrow(HPO:0005338) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of the eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) Sparse and thin eyebrow(HPO:0000535) Sparse lateral eyebrow(HPO:0005338) MedDRA: |
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Database Frequency: | 21 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
17q12 microdeletion syndrome | (Orphanet:261265) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Aicardi syndrome | (Orphanet:50) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Dubowitz syndrome | (Orphanet:235) |
Facial ectodermal dysplasia | (Orphanet:1807) |
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | (Orphanet:313846) |
Ichthyosis-cheek-eyebrow syndrome | (Orphanet:2267) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Kabuki syndrome | (Orphanet:2322) |
Oculotrichodysplasia | (Orphanet:2718) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Potocki-Shaffer syndrome | (Orphanet:52022) |
Renpenning syndrome | (Orphanet:3242) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE III | (OMIM:190351) |
Trichodermodysplasia - dental alterations | (Orphanet:3353) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |