Sparse eyelashes
Symptom Information:
Symptom ID: | HPO:0000653 | ||||||||
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) Sparse or absent eyelashes(HPO:0200102) Sparse eyelashes(HPO:0000653) 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) Sparse eyelashes(HPO:0000653) 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) Sparse eyelashes(HPO:0000653) MedDRA: |
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Database Frequency: | 58 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
19q13.11 microdeletion syndrome | (Orphanet:217346) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
DK1-CDG | (Orphanet:91131) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE | (OMIM:614929) |
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET | (OMIM:129540) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
EEM syndrome | (Orphanet:1897) |
Ectodermal dysplasia - syndactyly syndrome | (Orphanet:247820) |
Ectodermal dysplasia with natal teeth, Turnpenny type | (Orphanet:69083) |
Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome | (Orphanet:306542) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
HYPOTRICHOSIS 6 | (OMIM:607903) |
HYPOTRICHOSIS 7 | (OMIM:604379) |
HYPOTRICHOSIS 8 | (OMIM:278150) |
Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hidrotic ectodermal dysplasia, Christianson-Fourie type | (Orphanet:1808) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hypotrichosis simplex | (Orphanet:55654) |
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS | (OMIM:602540) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT | (OMIM:148210) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
KID syndrome | (Orphanet:477) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Lethal restrictive dermopathy | (Orphanet:1662) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
Marie Unna hereditary hypotrichosis | (Orphanet:444) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:257850) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Oculotrichodysplasia | (Orphanet:2718) |
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR | (OMIM:616099) |
Rosselli-Gulienetti syndrome | (Orphanet:90339) |
Skin fragility-woolly hair-palmoplantar keratoderma syndrome | (Orphanet:293165) |
Tetrasomy 12p | (Orphanet:884) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |
Yunis-Varon syndrome | (Orphanet:3472) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |