Abnormality of the periorbital region
Symptom Information:
| Symptom ID: | HPO:0000606 | ||||
| Synonyms: |
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| Quality: | |||||
| Cross references: |
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| Is a (Direct Parents): |
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| 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) MedDRA: |
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| Database Frequency: | 96 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 22q11.2 deletion syndrome | (Orphanet:567) |
| ADULT syndrome | (Orphanet:978) |
| Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
| Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
| Acromicric dysplasia | (Orphanet:969) |
| Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
| Alopecia | (Orphanet:79364) |
| Alopecia-intellectual deficit syndrome | (Orphanet:2850) |
| Alport syndrome | (Orphanet:63) |
| Ascher syndrome | (Orphanet:1253) |
| Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
| Benign familial infantile seizures | (Orphanet:306) |
| Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
| Cardiofaciocutaneous syndrome | (Orphanet:1340) |
| Cohen syndrome | (Orphanet:193) |
| Congenital hypothyroidism | (Orphanet:442) |
| Congenital hypothyroidism due to developmental anomaly | (Orphanet:95711) |
| Crandall syndrome | (Orphanet:202) |
| Deafness - enamel hypoplasia - nail defects | (Orphanet:3220) |
| Dermatomyositis | (Orphanet:221) |
| Dermo-odonto dysplasia | (Orphanet:1660) |
| Dyskeratosis congenita | (Orphanet:1775) |
| Ectodermal dysplasia syndrome | (Orphanet:79373) |
| Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
| Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
| FLOTCH syndrome | (Orphanet:2045) |
| Familial dysautonomia | (Orphanet:1764) |
| Fanconi anemia | (Orphanet:84) |
| Focal facial dermal dysplasia | (Orphanet:79133) |
| German syndrome | (Orphanet:2077) |
| Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
| Granulomatosis with polyangiitis | (Orphanet:900) |
| Griscelli disease | (Orphanet:381) |
| Hallermann-Streiff syndrome | (Orphanet:2108) |
| Hidrotic ectodermal dysplasia | (Orphanet:189) |
| Hidrotic ectodermal dysplasia, Christianson-Fourie type | (Orphanet:1808) |
| Hidrotic ectodermal dysplasia, Halal type | (Orphanet:1809) |
| Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
| Hypertrichosis cubiti - short stature | (Orphanet:2220) |
| Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
| Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
| Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
| Juvenile dermatomyositis | (Orphanet:93672) |
| Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
| Lassa fever | (Orphanet:99824) |
| Leprechaunism | (Orphanet:508) |
| Lethal restrictive dermopathy | (Orphanet:1662) |
| Leukonychia totalis | (Orphanet:2387) |
| Lipoid proteinosis | (Orphanet:530) |
| Mandibuloacral dysplasia | (Orphanet:2457) |
| Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
| Marie Unna hereditary hypotrichosis | (Orphanet:444) |
| Marshall syndrome | (Orphanet:560) |
| Melkersson-Rosenthal syndrome | (Orphanet:2483) |
| Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
| Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
| Monilethrix | (Orphanet:573) |
| Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
| Multiple endocrine neoplasia type 2 | (Orphanet:653) |
| Nager syndrome | (Orphanet:245) |
| Nasopalpebral lipoma - coloboma - telecanthus | (Orphanet:2399) |
| Neu-Laxova syndrome | (Orphanet:2671) |
| Neuroectodermal-endocrine syndrome | (Orphanet:2676) |
| Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
| Non-histaminic angioedema | (Orphanet:658) |
| Oculocutaneous albinism | (Orphanet:55) |
| Oculocutaneous albinism type 1B | (Orphanet:79434) |
| Oculomaxillofacial dysostosis | (Orphanet:1794) |
| Odontotrichomelic syndrome | (Orphanet:2723) |
| PARC syndrome | (Orphanet:2825) |
| Piebald trait - neurologic defects | (Orphanet:2885) |
| Piebaldism | (Orphanet:2884) |
| Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
| Relapsing polychondritis | (Orphanet:728) |
| Rombo syndrome | (Orphanet:3110) |
| Rothmund-Thomson syndrome | (Orphanet:2909) |
| Rothmund-Thomson syndrome type 1 | (Orphanet:221008) |
| Rothmund-Thomson syndrome type 2 | (Orphanet:221016) |
| Scalp-ear-nipple syndrome | (Orphanet:2036) |
| Schinzel-Giedion syndrome | (Orphanet:798) |
| Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
| Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
| Short tarsus - absence of lower eyelashes | (Orphanet:2832) |
| TRAPS syndrome | (Orphanet:32960) |
| Thymic carcinoma | (Orphanet:99868) |
| Thymic tumor | (Orphanet:100100) |
| Treacher-Collins syndrome | (Orphanet:861) |
| Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
| Triopia | (Orphanet:3374) |
| Waardenburg syndrome | (Orphanet:3440) |
| Waardenburg syndrome type 1 | (Orphanet:894) |
| Waardenburg-Shah syndrome | (Orphanet:897) |
| Waldenström macroglobulinemia | (Orphanet:33226) |
| Williams syndrome | (Orphanet:904) |
| Wyburn-Mason syndrome | (Orphanet:53719) |
| Xeroderma pigmentosum | (Orphanet:910) |