Poikiloderma

Symptom Information:

Symptom ID: HPO:0001029
Synonyms:
Poikiloderma (disorder) [Orphanet:23670]
Poikiloderma (morphologic abnormality) [Orphanet:23670]
Poikiloderma [Orphanet:23670]
Poikiloderma [OMIM:Poikiloderma]
Telangiectasic erythema/poikiloderma [Orphanet:23670]
Poikiloderma [MedDRA:10057041]
Poikiloderma (atrophic plaques with telangiectasia) [OMIM:Poikiloderma (atrophic plaques with telangiectasia)]
Quality:
Cross references:
Orphanet:23670 "Telangiectasic erythema/poikiloderma" [Orphanet:23670]
OMIM: "Poikiloderma" [OMIM:Poikiloderma]
OMIM: "Poikiloderma (atrophic plaques with telangiectasia)" [OMIM:Poikiloderma (atrophic plaques with telangiectasia)]
UMLS:C0392777 "Poikiloderma" [HPO:0001029]
UMLS:C0392777 "Poikiloderma" [Orphanet:23670]
Is a (Direct Parents):
HPO         Abnormality of skin morphology
MedDRA Skin and subcutaneous malformations and anomalies NEC
Orphanet Vascular skin abnormality
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)
                Abnormality of skin morphology(HPO:0011121)
                   Poikiloderma(HPO:0001029)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue disorders NEC(MedDRA:10040790)
       Skin and subcutaneous malformations and anomalies NEC(MedDRA:10040889)
          Poikiloderma(HPO:0001029)
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

Baller-Gerold syndrome (Orphanet:1225)
Classical mycosis fungoides (Orphanet:2584)
DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
Dermatomyositis (Orphanet:221)
Hereditary sclerosing poikiloderma, Weary type (Orphanet:221039)
Juvenile dermatomyositis (Orphanet:93672)
Kindler syndrome (Orphanet:2908)
PARC syndrome (Orphanet:2825)
POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY,AND PULMONARY FIBROSIS (OMIM:615704)
Piebald trait - neurologic defects (Orphanet:2885)
Poikiloderma with neutropenia (Orphanet:221046)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 1 (Orphanet:221008)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
Spastic paraplegia - neuropathy - poikiloderma (Orphanet:2821)
Xeroderma pigmentosum (Orphanet:910)
Xeroderma pigmentosum complementation group A (Orphanet:276249)
Xeroderma pigmentosum complementation group C (Orphanet:276255)
Xeroderma pigmentosum complementation group D (Orphanet:276258)
Xeroderma pigmentosum complementation group E (Orphanet:276261)
Xeroderma pigmentosum variant (Orphanet:90342)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)