Sparse or absent eyelashes

Symptom Information:

Symptom ID: HPO:0200102
Synonyms:
Partial to total absence of eyelashes [HPO:0200102]
SPARSE OR ABSENT EYELASHES [HPO:0200102]
SPARSE TO ABSENT EYELASHES [HPO:0200102]
Partial to total absence of eyelashes [OMIM:Partial to total absence of eyelashes]
Sparse or absent eyelashes [OMIM:Sparse or absent eyelashes]
Sparse to absent eyelashes [OMIM:Sparse to absent eyelashes]
Sparse/absent eyelashes [OMIM:Sparse/absent eyelashes]
Absent-sparse eyelashes [OMIM:Absent-sparse eyelashes]
Sparse to absent eyelashes (in some patients) [OMIM:Sparse to absent eyelashes (in some patients)]
Quality:
Cross references:
OMIM: "Partial to total absence of eyelashes" [OMIM:Partial to total absence of eyelashes]
OMIM: "Sparse or absent eyelashes" [OMIM:Sparse or absent eyelashes]
OMIM: "Sparse to absent eyelashes" [OMIM:Sparse to absent eyelashes]
OMIM: "Sparse/absent eyelashes" [OMIM:Sparse/absent eyelashes]
OMIM: "Absent-sparse eyelashes" [OMIM:Absent-sparse eyelashes]
OMIM: "Sparse to absent eyelashes (in some patients)" [OMIM:Sparse to absent eyelashes (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the eyelashes
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)
       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)
                         Sparse or absent eyelashes(HPO:0200102)
                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)
MedDRA:
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)