Abnormality of the eyelashes
Symptom Information:
Symptom ID: | HPO:0000499 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
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) 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) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) 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) |