Sparse or absent eyelashes
Symptom Information:
Symptom ID: | HPO:0200102 | |||||||||
Synonyms: |
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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 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 eyelid(HPO:0000492) Abnormality of the eyelashes(HPO:0000499) Sparse or absent eyelashes(HPO:0200102) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) Abnormality of the eyelashes(HPO:0000499) Sparse or absent eyelashes(HPO:0200102) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of the eyelashes(HPO:0000499) Sparse or absent eyelashes(HPO:0200102) MedDRA: |
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Database Frequency: | 64 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
17q11.2 microduplication syndrome | (Orphanet:139474) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Alopecia - epilepsy - pyorrhea - intellectual deficit | (Orphanet:1008) |
Alopecia antibody deficiency | (Orphanet:1006) |
Alopecia universalis | (Orphanet:701) |
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) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Choroidal atrophy - alopecia | (Orphanet:1433) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
Ectodermal dysplasia, tricho-odonto-onychial type | (Orphanet:1818) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
FLOTCH syndrome | (Orphanet:2045) |
Facial ectodermal dysplasia | (Orphanet:1807) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
Fried's tooth and nail syndrome | (Orphanet:99672) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
GAPO syndrome | (Orphanet:2067) |
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, Halal type | (Orphanet:1809) |
Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
Hypotrichosis simplex | (Orphanet:55654) |
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS | (OMIM:602540) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
KID syndrome | (Orphanet:477) |
Keratosis follicularis - dwarfism - cerebral atrophy | (Orphanet:2339) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Nager syndrome | (Orphanet:245) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Oculomaxillofacial dysostosis | (Orphanet:1794) |
Oculotrichodysplasia | (Orphanet:2718) |
Odontotrichomelic syndrome | (Orphanet:2723) |
Omphalocele syndrome, Shprintzen-Goldberg type | (Orphanet:3164) |
Pili torti - developmental delay - neurological abnormalities | (Orphanet:2891) |
Pseudoprogeria syndrome | (Orphanet:2985) |
Ptosis - upper ocular movement limitation - absence of lacrimal punctum | (Orphanet:228396) |
Satoyoshi syndrome | (Orphanet:3130) |
Short tarsus - absence of lower eyelashes | (Orphanet:2832) |
Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |
Toriello-Carey syndrome | (Orphanet:3338) |
Treacher-Collins syndrome | (Orphanet:861) |
Trichodental syndrome | (Orphanet:3351) |
Trichodermodysplasia - dental alterations | (Orphanet:3353) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
Trisomy 13 | (Orphanet:3378) |
Van Regemorter-Pierquin-Vamos syndrome | (Orphanet:3419) |
Vogt-Koyanagi-Harada disease | (Orphanet:3437) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Yunis-Varon syndrome | (Orphanet:3472) |