Absent eyebrow

Symptom Information:

Symptom ID: HPO:0002223
Synonyms:
Absent eyebrows [HPO:0002223]
Absent eyebrow (disorder) [Orphanet:6100]
Absent eyebrow [Orphanet:6100]
Absent eyebrows [OMIM:Absent eyebrows]
Absent/decreased/thin eyebrows [Orphanet:6100]
Absent eyebrows (in some patients) [OMIM:Absent eyebrows (in some patients)]
Eyebrows absent [OMIM:Eyebrows absent]
Quality:
Cross references:
Orphanet:6100 "Absent/decreased/thin eyebrows" [Orphanet:6100]
OMIM: "Absent eyebrows" [OMIM:Absent eyebrows]
OMIM: "Absent eyebrows (in some patients)" [OMIM:Absent eyebrows (in some patients)]
OMIM: "Eyebrows absent" [OMIM:Eyebrows absent]
UMLS:C0431448 "Absent eyebrow" [Orphanet:6100]
Is a (Direct Parents):
HPO         Absent hair
HPO         Aplasia/Hypoplasia of the eyebrow
Orphanet Abnormality of the eyebrow
Orphanet Sparse and thin eyebrow
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)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyebrow(HPO:0000534)
                      Aplasia/Hypoplasia of the eyebrow(HPO:0100840)
                         Absent eyebrow(HPO:0002223)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyebrow(HPO:0000534)
                      Aplasia/Hypoplasia of the eyebrow(HPO:0100840)
                         Absent eyebrow(HPO:0002223)
       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)
                      Absent eyebrow(HPO:0002223)
                Abnormal hair quantity(HPO:0011362)
                   Absent hair(HPO:0002298)
                      Absent eyebrow(HPO:0002223)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Ablepharon macrostomia syndrome (Orphanet:920)
Bartsocas-Papas syndrome (Orphanet:1234)
CARDIOFACIOCUTANEOUS SYNDROME 2 (OMIM:615278)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
Cardiofaciocutaneous syndrome (Orphanet:1340)
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
Fraser syndrome (Orphanet:2052)
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome (Orphanet:306542)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Keratosis follicularis - dwarfism - cerebral atrophy (Orphanet:2339)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
PARC syndrome (Orphanet:2825)
Pseudoprogeria syndrome (Orphanet:2985)
Pure hair and nail ectodermal dysplasia (Orphanet:69084)
Spastic paraplegia - neuropathy - poikiloderma (Orphanet:2821)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)