Aplasia/Hypoplasia of the skin

Symptom Information:

Symptom ID: HPO:0008065
Cross references:
Is a (Direct Parents):
HPO         Localized skin lesion
Is a (Whole tree): HPO:
    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)
Database Frequency: 81 / 7739

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)