Ectodermal dysplasia
Symptom Information:
| Symptom ID: | HPO:0000968 | ||
| Synonyms: |
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| 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 the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Ectodermal dysplasia(HPO:0000968) MedDRA: |
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| Database Frequency: | 46 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| ADULT syndrome | (Orphanet:978) |
| ANONYCHIA-ECTRODACTYLY | (OMIM:106900) |
| ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY | (OMIM:106990) |
| AREDYLD syndrome | (Orphanet:1133) |
| Absence of fingerprints - congenital milia | (Orphanet:1658) |
| Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema | (Orphanet:69088) |
| Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
| BRESEK syndrome | (Orphanet:85284) |
| Cerebellar ataxia - ectodermal dysplasia | (Orphanet:1174) |
| Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
| Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
| Contractures - ectodermal dysplasia - cleft lip/palate | (Orphanet:1484) |
| Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis | (Orphanet:352662) |
| Cranioectodermal dysplasia | (Orphanet:1515) |
| Cranioectodermal dysplasia 2 | (OMIM:613610) |
| Cranioectodermal dysplasia 3 | (OMIM:614099) |
| Cranioectodermal dysplasia 4 | (OMIM:614378) |
| Dermo-odonto dysplasia | (Orphanet:1660) |
| ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:614941) |
| ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE | (OMIM:614931) |
| ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET | (OMIM:129540) |
| ECTODERMAL DYSPLASIA WITH ADRENAL CYST | (OMIM:129550) |
| ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY | (OMIM:600906) |
| ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609944) |
| ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE | (OMIM:129810) |
| ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
| EEC syndrome | (Orphanet:1896) |
| EEM syndrome | (Orphanet:1897) |
| Ectodermal dysplasia - blindness | (Orphanet:1806) |
| Ectodermal dysplasia - cutaneous syndactyly syndrome | (Orphanet:247827) |
| Ectodermal dysplasia - syndactyly syndrome | (Orphanet:247820) |
| Ectodermal dysplasia with natal teeth, Turnpenny type | (Orphanet:69083) |
| Ectodermal dysplasia, tricho-odonto-onychial type | (Orphanet:1818) |
| Ellis Van Creveld syndrome | (Orphanet:289) |
| Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
| FOCAL FACIAL DERMAL DYSPLASIA 3, SETLEIS TYPE | (OMIM:227260) |
| Hidrotic ectodermal dysplasia | (Orphanet:189) |
| Hypohidrotic ectodermal dysplasia with immunodeficiency | (Orphanet:98813) |
| Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
| Odontotrichomelic syndrome | (Orphanet:2723) |
| Pilodental dysplasia - refractive errors | (Orphanet:2892) |
| Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
| TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES | (OMIM:273390) |
| Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
| Tricho-odonto-onychial dysplasia | (Orphanet:3355) |
| Zlotogora-Ogur syndrome | (Orphanet:3253) |