Alopecia
Symptom Information:
Symptom ID: | HPO:0001596 | ||||||||||||||||||||||||||||||
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 skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormal hair quantity(HPO:0011362) Alopecia(HPO:0001596) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Alopecia(HPO:0001596) Hypotrichosis(HPO:0001006) Alopecia(HPO:0001596) |
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Database Frequency: | 162 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q11.2 microduplication syndrome | (Orphanet:139474) |
3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY | (OMIM:210210) |
ADULT syndrome | (Orphanet:978) |
ALOPECIA, ANDROGENETIC, 1 | (OMIM:109200) |
ALOPECIA, CONGENITAL | (OMIM:300042) |
ANE syndrome | (Orphanet:157954) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Adams-Oliver syndrome | (Orphanet:974) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Alopecia | (Orphanet:79364) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Alopecia - epilepsy - pyorrhea - intellectual deficit | (Orphanet:1008) |
Alopecia - intellectual deficit - hypergonadotropic hypogonadism | (Orphanet:1014) |
Alopecia totalis | (Orphanet:700) |
Alopecia universalis | (Orphanet:701) |
Alopecia-intellectual deficit syndrome | (Orphanet:2850) |
Alpha heavy-chain disease | (Orphanet:100025) |
Alström syndrome | (Orphanet:64) |
Argininosuccinic aciduria | (Orphanet:23) |
Autoimmune polyendocrinopathy type 1 | (Orphanet:3453) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
Autosomal dominant Robinow syndrome | (Orphanet:3107) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal dominant palmoplantar keratoderma and congenital alopecia | (Orphanet:1010) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
BRESEK syndrome | (Orphanet:85284) |
Bathing suit ichthyosis | (Orphanet:100976) |
Biotinidase deficiency | (Orphanet:79241) |
Björnstad syndrome | (Orphanet:123) |
CANDIDIASIS, FAMILIAL, 1 | (OMIM:114580) |
CARASIL | (Orphanet:199354) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CHILD syndrome | (Orphanet:139) |
Cerebellar ataxia - ectodermal dysplasia | (Orphanet:1174) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Classical mycosis fungoides | (Orphanet:2584) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Congenital non-bullous ichthyosiform erythroderma | (Orphanet:79394) |
Cortisone reductase deficiency 1 | (OMIM:604931) |
Crandall syndrome | (Orphanet:202) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
DK1-CDG | (Orphanet:91131) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 | (OMIM:613990) |
Deafness - genital anomalies - metacarpal and metatarsal synostosis | (Orphanet:3224) |
Deafness-craniofacial syndrome | (Orphanet:3241) |
Distal monosomy 19p13.3 | (Orphanet:96129) |
Dorfman-Chanarin disease | (Orphanet:98907) |
Dyskeratosis congenita | (Orphanet:1775) |
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE | (OMIM:602032) |
ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE | (OMIM:614931) |
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET | (OMIM:129540) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
Epidermolysis bullosa simplex with anodontia/hypodontia | (Orphanet:2325) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Erosive pustular dermatosis of the scalp | (Orphanet:222) |
Erythrokeratodermia variabilis | (Orphanet:317) |
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | (Orphanet:313846) |
Fibrodysplasia ossificans progressiva | (Orphanet:337) |
Flynn-Aird syndrome | (Orphanet:2047) |
Focal dermal hypoplasia | (Orphanet:2092) |
Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
GAPO syndrome | (Orphanet:2067) |
Giant cell arteritis | (Orphanet:397) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Graham Little-Piccardi-Lassueur syndrome | (Orphanet:505) |
Gómez-López-Hernández syndrome | (Orphanet:1532) |
HYPOTRICHOSIS 4 | (OMIM:146550) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hepatoerythropoietic porphyria | (Orphanet:95159) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hyperandrogenism due to cortisone reductase deficiency | (Orphanet:168588) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Hypotrichosis simplex | (Orphanet:55654) |
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS | (OMIM:242150) |
IMMUNODEFICIENCY, COMMON VARIABLE, 10 | (OMIM:615577) |
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit | (Orphanet:2269) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Incontinentia pigmenti | (Orphanet:464) |
Ito hypomelanosis | (Orphanet:435) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Junctional epidermolysis bullosa, Herlitz type | (Orphanet:79404) |
Juvenile dermatomyositis | (Orphanet:93672) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
Keratoderma hereditarium mutilans | (Orphanet:494) |
Keratosis follicularis - dwarfism - cerebral atrophy | (Orphanet:2339) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Kerion celsi | (Orphanet:499) |
Keutel syndrome | (Orphanet:85202) |
Lethal acantholytic epidermolysis bullosa | (Orphanet:158687) |
Lichen planopilaris | (Orphanet:525) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Loose anagen syndrome | (Orphanet:168) |
MACS syndrome | (Orphanet:217335) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Marie Unna hereditary hypotrichosis | (Orphanet:444) |
Mixed connective tissue disease | (Orphanet:809) |
Monilethrix | (Orphanet:573) |
Moynahan syndrome | (Orphanet:2574) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Neuroectodermal-endocrine syndrome | (Orphanet:2676) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Odonto-onycho dysplasia - alopecia | (Orphanet:2722) |
Omenn syndrome | (Orphanet:39041) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
PARC syndrome | (Orphanet:2825) |
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 | (OMIM:615830) |
POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY,AND PULMONARY FIBROSIS | (OMIM:615704) |
Pachyonychia congenita | (Orphanet:2309) |
Pearson syndrome | (Orphanet:699) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Pili torti | (Orphanet:2889) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Primary cutaneous lymphoma | (Orphanet:542) |
Primary hypergonadotropic hypogonadism - partial alopecia | (Orphanet:2232) |
Pseudo-pelade of Brocq | (Orphanet:129) |
Pure hair and nail ectodermal dysplasia | (Orphanet:69084) |
Quinquaud's folliculitis decalvans | (Orphanet:346) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Rhizomelic chondrodysplasia punctata | (Orphanet:177) |
Rhizomelic chondrodysplasia punctata type 1 | (Orphanet:309789) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy | (Orphanet:169095) |
Severe combined immunodeficiency | (Orphanet:183660) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Sinus node disease and myopia | (OMIM:182190) |
Skin fragility-woolly hair-palmoplantar keratoderma syndrome | (Orphanet:293165) |
Sézary syndrome | (Orphanet:3162) |
TRAPS syndrome | (Orphanet:32960) |
TRICHOTILLOMANIA | (OMIM:613229) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
Thymoma | (Orphanet:99867) |
Transgrediens et progrediens palmoplantar keratoderma | (Orphanet:495) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Trichodysplasia - xeroderma | (Orphanet:3361) |
Ulerythema ophryogenesis | (Orphanet:3406) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
Werner syndrome | (Orphanet:902) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked agammaglobulinemia | (Orphanet:47) |
X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
Xeroderma pigmentosum | (Orphanet:910) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |