Abnormality of the eyebrow
Symptom Information:
| Symptom ID: | HPO:0000534 | ||||||
| Synonyms: |
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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) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyebrow(HPO:0000534) Abnormality of the periorbital region(HPO:0000606) 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) |