Long eyelashes
Symptom Information:
Symptom ID: | HPO:0000527 | |||||||||||||
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 eyelashes(HPO:0000499) Long eyelashes(HPO:0000527) 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 eyelid(HPO:0000492) Abnormality of the eyelashes(HPO:0000499) Long eyelashes(HPO:0000527) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyelid(HPO:0000492) Abnormality of the eyelashes(HPO:0000499) Long eyelashes(HPO:0000527) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Hypertrichoses(MedDRA:10020863) Long eyelashes(HPO:0000527) |
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Database Frequency: | 46 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
2p21 microdeletion syndrome | (Orphanet:163693) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acromicric dysplasia | (Orphanet:969) |
Amaurosis - hypertrichosis | (Orphanet:1021) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Blepharophimosis-intellectual deficit syndrome, Verloes type | (Orphanet:293725) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CORNELIA DE LANGE SYNDROME 2 | (OMIM:300590) |
CORNELIA DE LANGE SYNDROME 3 | (OMIM:610759) |
CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cornelia de Lange syndrome | (Orphanet:199) |
Costello syndrome | (Orphanet:3071) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Eyebrow duplication - syndactyly | (Orphanet:3172) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Floating-Harbor syndrome | (Orphanet:2044) |
GCS1-CDG | (Orphanet:79330) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
Hurler syndrome | (Orphanet:93473) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
KABUKI SYNDROME 2 | (OMIM:300867) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 | (OMIM:614607) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 | (OMIM:614608) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 16 | (OMIM:614609) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 | (OMIM:615009) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 | (OMIM:615866) |
MGAT2-CDG | (Orphanet:79329) |
Marden-Walker syndrome | (Orphanet:2461) |
Monosomy 22q13 | (Orphanet:48652) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 | (OMIM:615803) |
Roifman syndrome | (Orphanet:353298) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency | (Orphanet:353284) |
TMCO1 defect syndrome | (Orphanet:228407) |
Trichomegaly - cataract - hereditary spherocytosis | (Orphanet:3362) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
Wiedemann-Steiner syndrome | (Orphanet:319182) |