Aplasia/Hypoplasia of the eyebrow
Symptom Information:
Symptom ID: | HPO:0100840 | ||||||||
Synonyms: |
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Quality: | |||||||||
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) 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) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyebrow(HPO:0000534) Aplasia/Hypoplasia of the eyebrow(HPO:0100840) MedDRA: |
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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) |