Abnormality of the eyebrow

Symptom Information:

Symptom ID: HPO:0000534
Synonyms:
Eyebrow anomaly [Orphanet:6000]
Eyebrows anomalies [Orphanet:6000]
Quality:
Cross references:
Orphanet:6000 "Eyebrows anomalies" [Orphanet:6000]
Is a (Direct Parents):
HPO         obsolete Abnormality of the ocular region
HPO         Abnormality of the hair
HPO         Abnormality of the periorbital region
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:
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)