Abnormality of the eyebrow
Symptom Information:
Symptom ID: | HPO:0000534 | ||||||
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 eyebrow(HPO:0000534) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyebrow(HPO:0000534) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyebrow(HPO:0000534) MedDRA: |
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Database Frequency: | 39 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
1p36 deletion syndrome | (Orphanet:1606) |
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Amelogenesis imperfecta and gingival hyperplasia syndrome | (Orphanet:171836) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Böök syndrome | (Orphanet:1262) |
Central congenital hypothyroidism | (Orphanet:226298) |
Dyskeratosis congenita | (Orphanet:1775) |
Ectodermal dysplasia, Berlin type | (Orphanet:1816) |
Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
Eyebrow duplication - syndactyly | (Orphanet:3172) |
Focal facial dermal dysplasia | (Orphanet:79133) |
Griscelli disease | (Orphanet:381) |
Juberg-Hayward syndrome | (Orphanet:2319) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Monilethrix | (Orphanet:573) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Piebald trait - neurologic defects | (Orphanet:2885) |
Pili torti | (Orphanet:2889) |
Pilotto syndrome | (Orphanet:2894) |
Rombo syndrome | (Orphanet:3110) |
Rothmund-Thomson syndrome type 1 | (Orphanet:221008) |
Rothmund-Thomson syndrome type 2 | (Orphanet:221016) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Triopia | (Orphanet:3374) |
Ulerythema ophryogenesis | (Orphanet:3406) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Waardenburg-Shah syndrome | (Orphanet:897) |