Palpebral edema
Symptom Information:
Symptom ID: | HPO:0100540 | |||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||
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) Palpebral edema(HPO:0100540) Abnormality of facial soft tissue(HPO:0011799) Facial edema(HPO:0000282) Periorbital edema(HPO:0100539) Palpebral edema(HPO:0100540) Abnormality of the periorbital region(HPO:0000606) Periorbital edema(HPO:0100539) Palpebral edema(HPO:0100540) Abnormality of the eyelid(HPO:0000492) Palpebral edema(HPO:0100540) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of fluid regulation(HPO:0011032) Edema(HPO:0000969) Facial edema(HPO:0000282) Periorbital edema(HPO:0100539) Palpebral edema(HPO:0100540) MedDRA: Eye disorders(MedDRA:10015919) Ocular infections, irritations and inflammations(MedDRA:10021877) Lid, lash and lacrimal infections, irritations and inflammations(MedDRA:10024445) Palpebral edema(HPO:0100540) Eye disorders NEC(MedDRA:10015917) Ocular disorders NEC(MedDRA:10030032) Palpebral edema(HPO:0100540) |
|||||||||||||||||||||||||||||||||||||||
Database Frequency: | 31 / 7739 | |||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
14q12 microdeletion syndrome | (Orphanet:261144) |
AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION | (OMIM:204850) |
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Acromegaly | (Orphanet:963) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Blepharoptosis - myopia - ectopia lentis | (Orphanet:1259) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
Focal facial dermal dysplasia | (Orphanet:79133) |
GAPO syndrome | (Orphanet:2067) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
Hurler syndrome | (Orphanet:93473) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Intellectual deficit, X-linked, Shashi type | (Orphanet:85286) |
Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
MACS syndrome | (Orphanet:217335) |
Microlissencephaly - micromelia | (Orphanet:50810) |
Monosomy 22q13 | (Orphanet:48652) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Non-progressive cerebellar ataxia with intellectual deficit | (Orphanet:314647) |
PEHO syndrome | (Orphanet:2836) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
Pyknoachondrogenesis | (Orphanet:3003) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |