Ichthyosis
Symptom Information:
Symptom ID: | HPO:0008064 | ||||||||||||||||||||||||||||||||||||||
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) Thickened skin(HPO:0001072) Epidermal thickening(HPO:0011368) Ichthyosis(HPO:0008064) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Ichthyosis(HPO:0008064) Congenital, familial and genetic disorders(MedDRA:10010331) Skin and subcutaneous tissue disorders congenital(MedDRA:10040789) Skin and subcutaneous tissue disorders congenital NEC(MedDRA:10040834) Ichthyosis(HPO:0008064) |
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Database Frequency: | 108 / 7739 | ||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Acquired ichthyosis | (Orphanet:454) |
Acral self-healing collodion baby | (Orphanet:281127) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Alopecia-intellectual deficit syndrome | (Orphanet:2850) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autosomal recessive epidermolysis bullosa simplex | (Orphanet:89838) |
Bathing suit ichthyosis | (Orphanet:100976) |
Blau syndrome | (Orphanet:90340) |
Bloom syndrome | (Orphanet:125) |
Brachytelephalangic chondrodysplasia punctata | (Orphanet:79345) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CEDNIK syndrome | (Orphanet:66631) |
CHILD syndrome | (Orphanet:139) |
CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE | (OMIM:302950) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Congenital cataract - ichthyosis | (Orphanet:1376) |
Congenital ichthyosis - intellectual deficit - spastic quadriplegia | (Orphanet:352333) |
Congenital ichthyosis - microcephalus - tetraplegia | (Orphanet:2271) |
Congenital lethal erythroderma | (Orphanet:1954) |
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect | (Orphanet:280671) |
Congenital non-bullous ichthyosiform erythroderma | (Orphanet:79394) |
DERMATITIS, ATOPIC | (OMIM:603165) |
DK1-CDG | (Orphanet:91131) |
Deafness - enamel hypoplasia - nail defects | (Orphanet:3220) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Epidermolytic ichthyosis | (Orphanet:312) |
Exfoliative ichthyosis | (Orphanet:289586) |
Fanconi syndrome - ichthyosis - dysmorphism | (Orphanet:1981) |
Fetal Gaucher disease | (Orphanet:85212) |
Gaucher disease | (Orphanet:355) |
Genetic keratinization disorder associated with ocular features | (Orphanet:98697) |
Harlequin ichthyosis | (Orphanet:457) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS | (OMIM:242150) |
ICHTHYOSIS VULGARIS | (OMIM:146700) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7 | (OMIM:615022) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8 | (OMIM:613943) |
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS | (OMIM:602540) |
ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT | (OMIM:146750) |
ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA | (OMIM:242550) |
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit | (Orphanet:2269) |
Ichthyosis - hepatosplenomegaly - cerebellar degeneration | (Orphanet:2274) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Ichthyosis - intellectual deficit - dwarfism - renal impairment | (Orphanet:2278) |
Ichthyosis - oral and digital anomalies | (Orphanet:2272) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Ichthyosis hystrix gravior | (Orphanet:79504) |
Ichthyosis hystrix of Curth-Macklin | (Orphanet:79503) |
Ichthyosis prematurity syndrome | (Orphanet:88621) |
Ichthyosis-cheek-eyebrow syndrome | (Orphanet:2267) |
Ichthyosis-hypotrichosis syndrome | (Orphanet:91132) |
Infantile Refsum disease | (Orphanet:772) |
Intellectual deficit, X-linked - hypogonadism - ichthyosis - obesity - short stature | (Orphanet:85331) |
Intellectual deficit, X-linked - short stature - obesity | (Orphanet:3055) |
KID syndrome | (Orphanet:477) |
Kallmann syndrome | (Orphanet:478) |
Keratoderma hereditarium mutilans | (Orphanet:494) |
Keratoderma hereditarium mutilans with ichthyosis | (Orphanet:79395) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome | (Orphanet:281201) |
Keratosis palmaris et plantaris - clinodactyly | (Orphanet:86919) |
Keratosis pilaris atrophicans | (Orphanet:498) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Lamellar ichthyosis | (Orphanet:313) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
MACS syndrome | (Orphanet:217335) |
MEDNIK syndrome | (Orphanet:171851) |
MELAS | (Orphanet:550) |
Mal de Meleda | (Orphanet:87503) |
Muckle-Wells syndrome | (Orphanet:575) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Multiple sclerosis - ichthyosis - factor VIII deficiency | (Orphanet:3151) |
Multiple sulfatase deficiency | (Orphanet:585) |
NEU-LAXOVA SYNDROME 2 | (OMIM:616038) |
Netherton syndrome | (Orphanet:634) |
Neu-Laxova syndrome | (Orphanet:2671) |
Neuroectodermal-endocrine syndrome | (Orphanet:2676) |
Neutral lipid storage disease | (Orphanet:165) |
Nevus comedonicus syndrome | (Orphanet:64754) |
Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES | (OMIM:166740) |
Osteosclerosis - ichthyosis - premature ovarian failure | (Orphanet:75325) |
Pachyonychia congenita | (Orphanet:2309) |
Pityriasis rubra pilaris | (Orphanet:2897) |
REFSUM DISEASE, CLASSIC | (OMIM:266500) |
Recessive X-linked ichthyosis | (Orphanet:461) |
Refsum disease | (Orphanet:773) |
Rhizomelic chondrodysplasia punctata | (Orphanet:177) |
Rhizomelic chondrodysplasia punctata type 1 | (Orphanet:309789) |
SRD5A3-CDG | (Orphanet:324737) |
Self-healing collodion baby | (Orphanet:281122) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |
Superficial epidermolytic ichthyosis | (Orphanet:455) |
Syndromic X-linked ichthyosis | (Orphanet:281090) |
TRICHORRHEXIS NODOSA SYNDROME | (OMIM:275550) |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE | (OMIM:601675) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
X-linked Alport syndrome | (Orphanet:88917) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |
Zunich-Kaye syndrome | (Orphanet:3474) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |