Long eyelashes

Symptom Information:

Symptom ID: HPO:0000527
Synonyms:
Ciliary trichomegaly [HPO:0000527]
Unusually long eyelashes [HPO:0000527]
Trichomegaly [HPO:0000527]
Trichomegaly [Orphanet:7700]
Long eyelashes [OMIM:Long eyelashes]
Unusually long eyelashes [OMIM:Unusually long eyelashes]
Long/thick/curved lashes/trichomegaly/polytrichia [Orphanet:7700]
Trichomegaly [MedDRA:10044613]
Long eyelashes (2p21del) [OMIM:Long eyelashes (2p21del)]
Long eyelashes (54%) [OMIM:Long eyelashes (54%)]
Long eyelashes (59%) [OMIM:Long eyelashes (59%)]
Long eyelashes (in some patients) [OMIM:Long eyelashes (in some patients)]
Trichomegaly [OMIM:Trichomegaly]
Quality:
Cross references:
HPO:0011231 "Prominent eyelashes" [Orphanet:7700]
Orphanet:7700 "Long/thick/curved lashes/trichomegaly/polytrichia" [Orphanet:7700]
OMIM: "Long eyelashes" [OMIM:Long eyelashes]
OMIM: "Unusually long eyelashes" [OMIM:Unusually long eyelashes]
OMIM: "Long eyelashes (2p21del)" [OMIM:Long eyelashes (2p21del)]
OMIM: "Long eyelashes (54%)" [OMIM:Long eyelashes (54%)]
OMIM: "Long eyelashes (59%)" [OMIM:Long eyelashes (59%)]
OMIM: "Long eyelashes (in some patients)" [OMIM:Long eyelashes (in some patients)]
OMIM: "Trichomegaly" [OMIM:Trichomegaly]
UMLS:C0854699 "Trichomegaly" [HPO:0000527]
UMLS:C0854699 "Trichomegaly" [Orphanet:7700]
Is a (Direct Parents):
HPO         Abnormality of the eyelashes
MedDRA Hypertrichoses
HPO         Long lower 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)
                   Long eyelashes(HPO:0000527)
       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)
                         Long eyelashes(HPO:0000527)
                Abnormality of the periorbital region(HPO:0000606)
                   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)
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)