Aplasia/Hypoplasia of the eyebrow

Symptom Information:

Symptom ID: HPO:0100840
Synonyms:
SPARSE OR ABSENT EYEBROWS [HPO:0100840]
SPARSE TO ABSENT EYEBROWS [HPO:0100840]
Sparse/absent eyebrows [HPO:0100840]
Sparse or absent eyebrows [OMIM:Sparse or absent eyebrows]
Sparse to absent eyebrows [OMIM:Sparse to absent eyebrows]
Sparse/absent eyebrows [OMIM:Sparse/absent eyebrows]
Absent/sparse eyebrows [OMIM:Absent/sparse eyebrows]
Sparse to absent eyebrows (in some patients) [OMIM:Sparse to absent eyebrows (in some patients)]
Quality:
Cross references:
OMIM: "Sparse or absent eyebrows" [OMIM:Sparse or absent eyebrows]
OMIM: "Sparse to absent eyebrows" [OMIM:Sparse to absent eyebrows]
OMIM: "Sparse/absent eyebrows" [OMIM:Sparse/absent eyebrows]
OMIM: "Absent/sparse eyebrows" [OMIM:Absent/sparse eyebrows]
OMIM: "Sparse to absent eyebrows (in some patients)" [OMIM:Sparse to absent eyebrows (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the eyebrow
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)
                   Aplasia/Hypoplasia of the eyebrow(HPO:0100840)
       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)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyebrow(HPO:0000534)
                      Aplasia/Hypoplasia of the eyebrow(HPO:0100840)
MedDRA:
Database Frequency: 117 / 7739
Resource:

All diseases associated with this symptom:

17q11.2 microduplication syndrome (Orphanet:139474)
19q13.11 microdeletion syndrome (Orphanet:217346)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q37 microdeletion syndrome (Orphanet:1001)
8q22.1 microdeletion syndrome (Orphanet:178303)
AREDYLD syndrome (Orphanet:1133)
Ablepharon macrostomia syndrome (Orphanet:920)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Alopecia (Orphanet:79364)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Alopecia antibody deficiency (Orphanet:1006)
Alopecia universalis (Orphanet:701)
Alopecia-intellectual deficit syndrome (Orphanet:2850)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Barber-Say syndrome (Orphanet:1231)
Bartsocas-Papas syndrome (Orphanet:1234)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Björnstad syndrome (Orphanet:123)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Choroidal atrophy - alopecia (Orphanet:1433)
Crandall syndrome (Orphanet:202)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
Cronkhite-Canada syndrome (Orphanet:2930)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Facial ectodermal dysplasia (Orphanet:1807)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Fried's tooth and nail syndrome (Orphanet:99672)
Fronto-facio-nasal dysostosis (Orphanet:1791)
GAPO syndrome (Orphanet:2067)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
HYPOTRICHOSIS 11 (OMIM:615059)
HYPOTRICHOSIS 12 (OMIM:615885)
HYPOTRICHOSIS 8 (OMIM:278150)
Hair defect - photosensitivity - intellectual deficit (Orphanet:1408)
Hereditary hypotrichosis with recurrent skin vesicles (Orphanet:217407)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Hypotrichosis simplex (Orphanet:55654)
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit (Orphanet:2269)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Ichthyosis-cheek-eyebrow syndrome (Orphanet:2267)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Jacobsen syndrome (Orphanet:2308)
KBG syndrome (Orphanet:2332)
KID syndrome (Orphanet:477)
Keratosis follicularis - dwarfism - cerebral atrophy (Orphanet:2339)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Lamellar ichthyosis (Orphanet:313)
Lethal restrictive dermopathy (Orphanet:1662)
Marie Unna hereditary hypotrichosis (Orphanet:444)
Marshall syndrome (Orphanet:560)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Nager syndrome (Orphanet:245)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Netherton syndrome (Orphanet:634)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Oculomaxillofacial dysostosis (Orphanet:1794)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Omenn syndrome (Orphanet:39041)
Osteocraniostenosis (Orphanet:2763)
PACHYONYCHIA CONGENITA 2 (OMIM:167210)
PARC syndrome (Orphanet:2825)
Paternal 20q13.2q13.3 microdeletion syndrome (Orphanet:261304)
Pili torti - developmental delay - neurological abnormalities (Orphanet:2891)
Pseudo-pelade of Brocq (Orphanet:129)
Pseudoprogeria syndrome (Orphanet:2985)
Renpenning syndrome (Orphanet:3242)
Rombo syndrome (Orphanet:3110)
Rothmund-Thomson syndrome (Orphanet:2909)
Say-Barber-Miller syndrome (Orphanet:3132)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Spastic paraplegia - neuropathy - poikiloderma (Orphanet:2821)
Tetrasomy 12p (Orphanet:884)
Tietz syndrome (Orphanet:42665)
Toriello-Carey syndrome (Orphanet:3338)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
Trichodental syndrome (Orphanet:3351)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trichodysplasia - xeroderma (Orphanet:3361)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)
Vogt-Koyanagi-Harada disease (Orphanet:3437)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Woolly hair (Orphanet:170)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
X-linked mandibulofacial dysostosis (Orphanet:1131)
Yunis-Varon syndrome (Orphanet:3472)
Zlotogora-Ogur syndrome (Orphanet:3253)