Poikiloderma
Symptom Information:
Symptom ID: | HPO:0001029 | |||||||
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) 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) |
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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) |