Thickened skin
Symptom Information:
Symptom ID: | HPO:0001072 | |||||||||||||||||||||||||||||
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) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Thickened skin(HPO:0001072) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Skin hyperplasias and hypertrophies(MedDRA:10040866) Thickened skin(HPO:0001072) |
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Database Frequency: | 87 / 7739 | |||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Absence of fingerprints - congenital milia | (Orphanet:1658) |
Acquired epidermolysis bullosa | (Orphanet:46487) |
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Acrocephalopolydactyly | (Orphanet:221054) |
Acrocephalosyndactyly | (Orphanet:946) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Acromegaly | (Orphanet:963) |
Acromicric dysplasia | (Orphanet:969) |
Acroosteolysis, dominant type | (Orphanet:955) |
Alström syndrome | (Orphanet:64) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
CREST syndrome | (Orphanet:90290) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Congenital hypothyroidism | (Orphanet:442) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Cutaneous mastocytoma | (Orphanet:79455) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
DERMATOLEUKODYSTROPHY | (OMIM:221790) |
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES | (OMIM:127200) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Darier disease | (Orphanet:218) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Dermatofibrosarcoma protuberans | (Orphanet:31112) |
Dermatoleukodystrophy | (Orphanet:1659) |
Diffuse cutaneous mastocytosis | (Orphanet:79456) |
Diffuse palmoplantar keratoderma-acrocyanosis syndrome | (Orphanet:86918) |
Familial Dupuytren contracture | (Orphanet:79142) |
Fetal Gaucher disease | (Orphanet:85212) |
GELEOPHYSIC DYSPLASIA 1 | (OMIM:231050) |
GELEOPHYSIC DYSPLASIA 2 | (OMIM:614185) |
Gaucher disease type 2 | (Orphanet:77260) |
Geleophysic dysplasia | (Orphanet:2623) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Haim-Munk syndrome | (Orphanet:2342) |
Hereditary palmoplantar keratoderma | (Orphanet:79357) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Inherited epidermolysis bullosa | (Orphanet:79361) |
Intestinal lymphangiectasia | (Orphanet:36204) |
Isolated punctate palmoplantar keratoderma | (Orphanet:2338) |
Juvenile idiopathic arthritis | (Orphanet:92) |
KID syndrome | (Orphanet:477) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Leprechaunism | (Orphanet:508) |
Leri pleonosteosis | (Orphanet:2900) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
Lipoid proteinosis | (Orphanet:530) |
MUCOLIPIDOSIS III ALPHA/BETA | (OMIM:252600) |
Melorheostosis | (Orphanet:2485) |
Menkes disease | (Orphanet:565) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Mucolipidosis type 3 | (Orphanet:577) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Myalgia-eosinophilia syndrome associated with tryptophan | (Orphanet:2582) |
Myhre syndrome | (Orphanet:2588) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Oculocutaneous albinism type 1B | (Orphanet:79434) |
Omenn syndrome | (Orphanet:39041) |
PMM2-CDG | (Orphanet:79318) |
POEMS syndrome | (Orphanet:2905) |
Pachydermoperiostosis | (Orphanet:2796) |
Palmoplantar keratoderma-spastic paralysis syndrome | (Orphanet:2201) |
Parana hard-skin syndrome | (Orphanet:2812) |
Pityriasis rubra pilaris | (Orphanet:2897) |
Primary cutis verticis gyrata | (Orphanet:671) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Proteus syndrome | (Orphanet:744) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Scleroderma | (Orphanet:801) |
Secondary intestinal lymphangiectasia | (Orphanet:90363) |
Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
Stern-Lubinsky-Durrie syndrome | (Orphanet:3194) |
Stiff skin syndrome | (Orphanet:2833) |
Torg-Winchester syndrome | (Orphanet:3460) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
Xeroderma pigmentosum | (Orphanet:910) |