Ichthyosis

Symptom Information:

Symptom ID: HPO:0008064
Synonyms:
Hypertrophic ichthyosis [HPO:0008064]
Ichthyosiform abnormality of the skin [HPO:0008064]
Ichthyotic skin [HPO:0008064]
Congenital ichthyosis of skin [HPO:0008064]
Congenital ichthyosis of skin (disorder) [Orphanet:23180]
Ichthyoses [Orphanet:23180]
Congenital ichthyosis [Orphanet:23180]
Dermatitis ichthyosiform [Orphanet:23180]
Ichthyosis [OMIM:Ichthyosis]
Ichthyotic skin [OMIM:Ichthyotic skin]
Ichthyosis/ichthyosiform dermatitis [Orphanet:23180]
Ichthyosis congenita [Orphanet:23180]
Ichthyosis [Orphanet:23180]
Ichthyosis congenital [Orphanet:23180]
Ichthyosis [MedDRA:10021198]
Bullous ichthyosiform erythroderma [MedDRA:10021198]
Congenital ichthyosis [MedDRA:10021198]
Epidermolytic hyperkeratosis [MedDRA:10021198]
Ichthyosis congenita [MedDRA:10021198]
Ichthyosis congenital [MedDRA:10021198]
Ichthyosis inherited [MedDRA:10021198]
Ichthyosis vulgaris [MedDRA:10021198]
Lamellar ichthyosis [MedDRA:10021198]
X-linked ichthyosis [MedDRA:10021198]
Ichthyosis aggravated [MedDRA:10021198]
Ichthyosis acquired [MedDRA:10021199]
Acquired ichthyosis [MedDRA:10021199]
Dermatitis ichthyosiform [MedDRA:10021199]
Ichthyosis senile [MedDRA:10021199]
Senile ichthyosis [MedDRA:10021199]
Skin change ichthyosiform [MedDRA:10021199]
Ichthyosiform dermatitis [OMIM:Ichthyosiform dermatitis]
Ichthyosis (in contiguous gene syndrome patients) [OMIM:Ichthyosis (in contiguous gene syndrome patients)]
Ichthyosis (in some patients) [OMIM:Ichthyosis (in some patients)]
Ichthyosis (rare) [OMIM:Ichthyosis (rare)]
Ichthyosis vulgaris [OMIM:Ichthyosis vulgaris]
Lamellar ichthyosis [OMIM:Lamellar ichthyosis]
Ichthyoses [MedDRA:10021197]
Quality:
Cross references:
Orphanet:23180 "Ichthyosis/ichthyosiform dermatitis" [Orphanet:23180]
OMIM: "Ichthyosis" [OMIM:Ichthyosis]
OMIM: "Ichthyotic skin" [OMIM:Ichthyotic skin]
OMIM: "Ichthyosiform dermatitis" [OMIM:Ichthyosiform dermatitis]
OMIM: "Ichthyosis (in contiguous gene syndrome patients)" [OMIM:Ichthyosis (in contiguous gene syndrome patients)]
OMIM: "Ichthyosis (in some patients)" [OMIM:Ichthyosis (in some patients)]
OMIM: "Ichthyosis (rare)" [OMIM:Ichthyosis (rare)]
OMIM: "Ichthyosis vulgaris" [OMIM:Ichthyosis vulgaris]
OMIM: "Lamellar ichthyosis" [OMIM:Lamellar ichthyosis]
UMLS:C0020758 "Ichthyosis" [HPO:0008064]
UMLS:C0020757 "Ichthyoses" [Orphanet:23180]
UMLS:C0020758 "Congenital ichthyosis" [Orphanet:23180]
UMLS:C0859053 "Dermatitis ichthyosiform" [Orphanet:23180]
Is a (Direct Parents):
HPO         Epidermal thickening
MedDRA Skin and subcutaneous tissue disorders congenital NEC
Orphanet Abnormality of the skin
MedDRA Cornification and dystrophic skin disorders
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)
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)