Aplasia/Hypoplasia of the skin
Symptom Information:
| Symptom ID: | HPO:0008065 | ||
| 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 the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Localized skin lesion(HPO:0011355) Aplasia/Hypoplasia of the skin(HPO:0008065) MedDRA: |
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| Database Frequency: | 81 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Acral dystrophic epidermolysis bullosa | (Orphanet:158673) |
| Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
| Acrogeria | (Orphanet:2500) |
| Adams-Oliver syndrome | (Orphanet:974) |
| Aplasia cutis - myopia | (Orphanet:1117) |
| Ataxia-telangiectasia | (Orphanet:100) |
| Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
| Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
| Barber-Say syndrome | (Orphanet:1231) |
| Branchio-oculo-facial syndrome | (Orphanet:1297) |
| Circumscribed cutaneous aplasia of the vertex | (Orphanet:1114) |
| Cockayne syndrome | (Orphanet:191) |
| Curry-Jones syndrome | (Orphanet:1553) |
| Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
| De Barsy syndrome | (Orphanet:2962) |
| Dermatomyositis | (Orphanet:221) |
| Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
| Desmosterolosis | (Orphanet:35107) |
| Disseminated superficial actinic porokeratosis | (Orphanet:79152) |
| Dyskeratosis congenita | (Orphanet:1775) |
| Dysosteosclerosis | (Orphanet:1782) |
| Dystrophic epidermolysis bullosa | (Orphanet:303) |
| EEC syndrome | (Orphanet:1896) |
| Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
| Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
| Epidermolysis bullosa simplex superficialis | (Orphanet:89839) |
| Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
| Epidermolysis bullosa simplex, Dowling-Meara type | (Orphanet:79396) |
| Epidermolysis bullosa simplex, Ogna type | (Orphanet:79401) |
| Exostoses - anetodermia - brachydactyly type E | (Orphanet:1962) |
| Facial ectodermal dysplasia | (Orphanet:1807) |
| Flynn-Aird syndrome | (Orphanet:2047) |
| Focal dermal hypoplasia | (Orphanet:2092) |
| Focal facial dermal dysplasia | (Orphanet:79133) |
| Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
| Hallermann-Streiff syndrome | (Orphanet:2108) |
| Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
| Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
| Hereditary thrombophilia due to congenital protein S deficiency | (Orphanet:743) |
| Hyperkeratosis lenticularis perstans | (Orphanet:409) |
| Junctional epidermolysis bullosa | (Orphanet:305) |
| Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
| Juvenile hyaline fibromatosis | (Orphanet:2028) |
| Keutel syndrome | (Orphanet:85202) |
| Kindler syndrome | (Orphanet:2908) |
| Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
| Lichen planopilaris | (Orphanet:525) |
| Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
| Lyme disease | (Orphanet:91546) |
| Malignant atrophic papulosis | (Orphanet:679) |
| Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
| Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
| Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
| Nodular non-suppurative panniculitis | (Orphanet:33577) |
| Oculocerebrocutaneous syndrome | (Orphanet:1647) |
| PARC syndrome | (Orphanet:2825) |
| Palmoplantar keratoderma-sclerodactyly syndrome | (Orphanet:384) |
| Porokeratosis | (Orphanet:79358) |
| Porokeratosis of Mibelli | (Orphanet:735) |
| Porokeratosis plantaris palmaris et disseminata | (Orphanet:737) |
| Primary cutaneous lymphoma | (Orphanet:542) |
| Primary lipodystrophy | (Orphanet:90970) |
| Progressive hemifacial atrophy | (Orphanet:1214) |
| Prolidase deficiency | (Orphanet:742) |
| Recessive aplasia cutis congenita of limbs | (Orphanet:1115) |
| Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
| Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
| Rombo syndrome | (Orphanet:3110) |
| Rothmund-Thomson syndrome | (Orphanet:2909) |
| Rothmund-Thomson syndrome type 1 | (Orphanet:221008) |
| Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
| Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |
| Stiff skin syndrome | (Orphanet:2833) |
| Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |
| Ulerythema ophryogenesis | (Orphanet:3406) |
| Werner syndrome | (Orphanet:902) |
| X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
| Xeroderma pigmentosum | (Orphanet:910) |
| Xeroderma pigmentosum variant | (Orphanet:90342) |
| Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |
| Xp22.3 microdeletion syndrome | (Orphanet:1643) |