Sparse eyelashes

Symptom Information:

Symptom ID: HPO:0000653
Synonyms:
Scant eyelashes [HPO:0000653]
Scanty eyelashes [HPO:0000653]
Scant eyelashes [OMIM:Scant eyelashes]
Scanty eyelashes [OMIM:Scanty eyelashes]
Sparse eyelashes [OMIM:Sparse eyelashes]
Absent/decreased lashes [Orphanet:7800]
Sparse eyelashes (classic feature) [OMIM:Sparse eyelashes (classic feature)]
Sparse eyelashes (in some patients) [OMIM:Sparse eyelashes (in some patients)]
Quality:
Cross references:
Orphanet:7800 "Absent/decreased lashes" [Orphanet:7800]
OMIM: "Scant eyelashes" [OMIM:Scant eyelashes]
OMIM: "Scanty eyelashes" [OMIM:Scanty eyelashes]
OMIM: "Sparse eyelashes" [OMIM:Sparse eyelashes]
OMIM: "Sparse eyelashes (classic feature)" [OMIM:Sparse eyelashes (classic feature)]
OMIM: "Sparse eyelashes (in some patients)" [OMIM:Sparse eyelashes (in some patients)]
Is a (Direct Parents):
HPO         Sparse or absent eyelashes
Orphanet Absent eyelashes
HPO         Sparse upper eyelashes
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)
                            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)
       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)
MedDRA:
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)