Abnormality of the eyelashes

Symptom Information:

Symptom ID: HPO:0000499
Synonyms:
Eyelash abnormality [HPO:0000499]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of upper eyelashes
HPO         Abnormality of the eyelid
HPO         Abnormality of lower eyelashes
HPO         Abnormality of the hair
HPO         Ectopic cilia of eyelid
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)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Abnormality of the eyelashes(HPO:0000499)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
                      Abnormality of the eyelashes(HPO:0000499)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the hair(HPO:0001595)
                Abnormality of the eyelashes(HPO:0000499)
MedDRA:
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2p21 microdeletion syndrome (Orphanet:163693)
4q21 microdeletion syndrome (Orphanet:238750)
Acro-cardio-facial syndrome (Orphanet:2008)
Amaurosis - hypertrichosis (Orphanet:1021)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive chorioretinopathy-microcephaly (Orphanet:2518)
Coffin-Siris syndrome (Orphanet:1465)
Cohen syndrome (Orphanet:193)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Cornelia de Lange syndrome (Orphanet:199)
Desbuquois syndrome (Orphanet:1425)
Distal trisomy 6p (Orphanet:1745)
Eyebrow duplication - syndactyly (Orphanet:3172)
Facial ectodermal dysplasia (Orphanet:1807)
Fine-Lubinsky syndrome (Orphanet:1272)
Floating-Harbor syndrome (Orphanet:2044)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Jacobsen syndrome (Orphanet:2308)
Kabuki syndrome (Orphanet:2322)
MEHMO syndrome (Orphanet:85282)
Monosomy 22q13 (Orphanet:48652)
Non-distal trisomy 13q (Orphanet:1702)
Okamoto syndrome (Orphanet:2729)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Progeroid syndrome, Petty type (Orphanet:2963)
Rombo syndrome (Orphanet:3110)
Schwartz-Jampel syndrome (Orphanet:800)
Short stature - wormian bones - dextrocardia (Orphanet:2863)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)