| 疾病名称 |
别名 |
|
| Monilethrix |
|
Beaded Hair
|
MNLIX
|
|
Nodose Hair
|
Moniliform Hair Syndrome
|
|
|
| Hair Disease |
|
Hair Diseases
|
Hair Anomaly
|
|
Hair Disorder
|
Hair Problems
|
|
|
| Black Piedra |
|
Tinea Nodosa
|
Trichomycosis Nodularis
|
|
Chignon Disease
|
|
|
| Keratosis |
|
Actinic Keratosis
|
Hyperkeratosis
|
|
|
| Hypotrichosis 6 |
|
HYPT6
|
Lah1
|
|
Hypotrichosis, Localized, Autosomal Recessive
|
Monilethrix-Like Hypotrichosis
|
|
Hypotrichosis, Localized, Autosomal Recessive 1
|
Lah
|
|
Htl
|
Autosomal Recessive Localized Hypotrichosis
|
|
Hypotrichosis Localized Autosomal Recessive
|
Hypotrichosis Localized Autosomal Recessive 1
|
|
Hypotrichosis, Type 6
|
|
|
| White Sponge Nevus 1 |
|
White Sponge Nevus Of Cannon
|
Leukokeratosis, Hereditary Mucosal
|
|
Hereditary Mucosal Leukokeratosis
|
White Sponge Nevus
|
|
WSN1
|
Wsn
|
|
Cannon'S Disease
|
Familial White Folded Mucosal Dysplasia
|
|
Hereditary Leukokeratosis
|
Hereditary Oral Keratosis
|
|
Leukokeratosis Of Oral Mucosa
|
Nevus Of Cannon
|
|
White Folded Gingivostomatosis
|
White Gingivostomatitis
|
|
White Sponge Naevus
|
White Sponge Nevus Of Mucosa
|
|
|
| Naegeli-Franceschetti-Jadassohn Syndrome |
|
Naegeli Syndrome
|
Nfj Syndrome
|
|
NFJS
|
Reticular Skin Changes, Dental Anomalies, Decreased Function Of Sweat Glands, Strabismus, And Optic Atrophy
|
|
Naegeli-Franceschetti-Jadassohn Syndrome/Dermatopathia Pigmentosa Reticularis
|
Dpr
|
|
Franceschetti-Jadassohn Syndrome
|
Nfjs/Dpr
|
|
|
| Hypotrichosis |
|
|
| Alopecia |
|
|
| Epidermolytic Hyperkeratosis |
|
Bullous Congenital Ichthyosiform Erythroderma
|
Bullous Ichthyosiform Erythroderma
|
|
EHK
|
Bullous Erythroderma Ichthyosiformis Congenita Of Brocq
|
|
Bcie
|
Bie
|
|
Epidermolytic Ichthyosis
|
Ichthyosis Bullosa Of Siemens
|
|
Superficial Epidermolytic Ichthyosis
|
Hyperkeratosis, Epidermolytic
|
|
Congenital Bullous Ichthyosiform Erythroderma
|
Bullous Type Ichthyosis
|
|
Epidermolytic Palmoplantar Hyperkeratosis
|
Bullous Ichthyosiform Erythroderma Congenita
|
|
Bullous Erythroderma Ichthyosiforme
|
Sei
|
|
Epidermolytic Hyperkeratosis Late-Onset
|
Epidermolytic Hyperkeratosis, Late-Onset
|
|
|
| Loose Anagen Hair Syndrome |
|
Loose Anagen Syndrome
|
LAHS
|
|
|
| Diffuse Alopecia Areata |
|
|
| Ectodermal Dysplasia 4, Hair/Nail Type |
|
Pure Hair And Nail Ectodermal Dysplasia
|
ECTD4
|
|
Ectodermal Dysplasia, Pure Hair-Nail Type
|
Ectodermal Dysplasia, 'Pure' Hair/Nail Type
|
|
Hned
|
Hair-Nail Ectodermal Dysplasia
|
|
Phned
|
Ectodermal Dysplasia Pure Hair-Nail Type
|
|
Ectodermal Dysplasia, 'Pure' Hair-Nail Type
|
Dysplasia, Ectodermal, Type 4, Hair/Nail
|
|
|
| T-Cell Immunodeficiency, Congenital Alopecia, And Nail Dystrophy |
|
Winged Helix Deficiency
|
Alymphoid Cystic Thymic Dysgenesis
|
|
Severe T-Cell Immunodeficiency-Congenital Alopecia-Nail Dystrophy Syndrome
|
Pignata Guarino Syndrome
|
|
TIDAND
|
T-Cell Immunodeficiency, Congenital Alopecia And Nail Dystrophy
|
|
Congenital Alopecia And Nail Dystrophy Associated With Severe Functional T-Cell Immunodeficiency
|
Severe Combined Immunodeficiency Due To Foxn1 Deficiency
|
|
Foxn1 Deficiency
|
Nude/Scid
|
|
Nude/Severe Combined Immunodeficiency
|
Scid Due To Foxn1 Deficiency
|
|
Severe T-Cell Immunodeficiency-Congenital Alopecia-Nail Dystrophy
|
|
|
| Loeys-Dietz Syndrome 3 |
|
LDS3
|
Aneurysms-Osteoarthritis Syndrome
|
|
Loeys-Dietz Syndrome With Osteoarthritis
|
Aneurysm-Osteoarthritis Syndrome
|
|
Lds1c
|
Loeys-Dietz Syndrome, Type 3
|
|
Loeys-Dietz Syndrome, Type 1c, Formerly
|
Lds1c, Formerly
|
|
Loeys-Dietz Syndrome Type 1c
|
Loeys-Dietz Syndrome Type 3
|
|
Aneurysm - Osteoarthritis Syndrome
|
Loeys-Dietz Syndrome, Type 1c
|
|
Aos
|
Loeys-Dietz Syndrome 1c
|
|
|
| Palmoplantar Keratoderma, Epidermolytic |
|
Epidermolytic Palmoplantar Keratoderma
|
EPPK
|
|
Keratosis Palmaris Et Plantaris Familiaris
|
Tylosis
|
|
Keratosis Of Greither
|
Diffuse Nonepidermolytic Palmoplantar Keratoderma
|
|
Keratoderma, Palmoplantar, Epidermolytic
|
Unna-Thost Palmoplantar Keratoderma
|
|
Epidermolytic Palmoplantar Keratoderma Of Voerner
|
Ppke
|
|
Keratoderma, Epidermolytic Palmoplantar
|
Palmoplantar Keratoderma, Vorner Type
|
|
Hyperkeratosis, Localized Epidermolytic
|
Diffuse Erythrodermic Palmoplantar Keratoderma, Vörner Type
|
|
Epidermolytic Palmoplantar Keratoderma Of Vörner
|
Hyperkeratosis Palmoplantar Localized Epidermolytic
|
|
Diffuse Neppk
|
Ppk Diffusa Circumscripta
|
|
Thost-Unna Disease
|
Thost-Unna Palmoplantar Keratoderma
|
|
Diffuse Erythrodermic Palmoplantar Keratoderma, Voerner Type
|
Diffuse Erythrodermic Palmoplantar Keratoderma, Vorner Type
|
|
Epidermolytic Palmoplantar Keratoderma Of Vorner
|
Ehppk
|
|
Epidermolytic Unna-Thost Disease
|
Localized Epidermolytic Hyperkeratosis
|
|
Palmoplantar Keratoderma Vorner Type
|
Unilateral Palmoplantar Verrucous Nevus
|
|
UPVN
|
Keratoderma, Palmoplantar, Diffuse
|
|
Hyperkeratosis
|
Palmoplantar Keratoderma, Nonepidermolytic
|
|
Epidermolytic Palmoplantar Keratoderma Vorner Type
|
Type B Tylosis
|
|
Hyperkeratosis Of The Palms And Soles And Esophageal Papillomas
|
Type A Tylosis
|
|
|
| Steatocystoma Multiplex |
|
Sebocystomatosis
|
Multiple Sebaceous Cysts
|
|
Multiplex Steatocystoma
|
Sebaceous Cysts, Multiple
|
|
SM
|
|
|
| Atrichia With Papular Lesions |
|
Papular Atrichia
|
APL
|
|
Congenital Atrichia
|
|
|
| Agnathia-Otocephaly Complex |
|
Otocephaly
|
Holoprosencephaly-Agnathia
|
|
Dysgnathia Complex Agnathia-Holoprosencephaly
|
AGOTC
|
|
Agnathia-Holoprosencephaly-Situs Inversus Syndrome
|
Dysgnathia Complex
|
|
Agnathia-Holoprosencephaly
|
Cervical Auricle
|
|
|
| White Piedra |
|
Tinea Blanca
|
Trichosporosis Nodosa
|
|
|
| Microphthalmia, Syndromic 6 |
|
MCOPS6
|
Microphthalmia And Pituitary Anomalies
|
|
Microphthalmia With Brain And Digit Anomalies
|
Microphthalmia With Brain And Digit Developmental Anomalies
|
|
Syndromic Microphthalmia Type 6
|
Syndromic Microphthalmia 6
|
|
Anophthalmia Clinical With Micrognathia Malformed Ears Digital Anomalies And Abnormal External Genitalia
|
Bakrania-Ragge Syndrome
|
|
Orofacial Cleft 11
|
Anophthalmia, Clinical, With Micrognathia, Malformed Ears, Digital Anomalies, And Abnormal External Genitalia
|
|
Microphthalmia Syndromic 6
|
Microphthalmia, Syndromic, 6
|
|
Clinical Anophthalmia With Micrognathia, Malformed Ears, Digital Anomalies And Abnormal External Genitalia
|
Microphthalmia Syndromic, Type 6
|
|
|
| Epidermolysis Bullosa Simplex 2f, With Mottled Pigmentation |
|
Epidermolysis Bullosa Simplex With Mottled Pigmentation
|
Ebsmp
|
|
Speckled Hyperpigmentation With Punctate Palmoplantar Keratoses And Childhood Blistering
|
Ebs-Mp
|
|
EBS2F
|
Ebs With Mottled Pigmentation
|
|
Epidermolysis Bullosa Simplex-Mp
|
Speckled Hyperpigmentation, Palmo-Plantar Punctate Keratoses And Childhood Blistering
|
|
Epidermolysis Bullosa Simplex, With Mottled Pigmentation
|
|
|
| Dermatopathia Pigmentosa Reticularis |
|
|
| Ichthyosis |
|
Ichthyoses
|
Non-Syndromic Ichthyosis
|
|
Congenital Ichthyosis
|
|
|
| Sucrase-Isomaltase Deficiency, Congenital |
|
Congenital Sucrase-Isomaltase Deficiency
|
CSID
|
|
Si Deficiency
|
Congenital Sucrose Intolerance
|
|
Disaccharide Intolerance
|
Sucrase-Isomaltase Deficiency
|
|
Disaccharide Intolerance I
|
Congenital Sucrose-Isomaltose Malabsorption
|
|
Sucrose-Isomaltose Malabsorption, Congenital
|
Sucrose Intolerance, Congenital
|
|
Congenital Sucrase-Isomaltose Malabsorption
|
Congenital Sucrose-Isomaltase Malabsorption
|
|
Disaccharide Intolerance, 1
|
Sucrose Intolerance Congenital
|
|
Sucrose-Isomaltase Malabsorption, Congenital
|
Disaccharidase Deficiency
|
|
Invertase Deficiency
|
Sucrase-Alpha-Dextrinase Deficiency
|
|
Disaccharide Intolerance Type I
|
Csid - [Congenital Sucrase-Isomaltase Deficiency]
|
|
Sucrose Intolerance Of Newborn
|
Sucrose Intolerance
|
|
Sucrase Deficiency
|
Disaccharide Malabsorption
|
|
Intestinal Disaccharidase Deficiency
|
|
|
| Pachyonychia Congenita 1 |
|
Pachyonychia Congenita
|
Jadassohn-Lewandowsky Syndrome
|
|
Pachyonychia Congenita Syndrome
|
PC1
|
|
Pachyonychia Congenita, Jadassohn-Lewandowsky Type
|
Congenital Pachyonychia
|
|
Pachyonychia Congenita, Type 1
|
Pachyonychia Congenita, Jadassohn-Lewandowsky Type, Formerly
|
|
Jadassohn-Lewandowsky Syndrome, Formerly
|
Jackson-Lawler Type Pachyonychia Congenita
|
|
Pachyonychia Congenita Type 1
|
Jackson-Lawler Syndrome
|
|
Jadassohn-Lewandowski Syndrome
|
Pc
|
|
Pachyonychia Congenita Jackson-Lawler Type
|
Pachyonychia Congenita Jadassohn-Lewandowsky Type
|
|
Pachyonychia Congenita Jackson Lawler Type
|
Pc-1
|
|
Pachyonychia Congenita, Jadassohn Lewandowsky Type
|
Pachyonychia Congenita, Type 2
|
|
|
| Hypotrichosis 2 |
|
HYPT2
|
Hypotrichosis Simplex Of The Scalp 1
|
|
Htss1
|
Htss
|
|
Hypotrichosis, Spanish Type
|
Spanish Type Hypotrichosis
|
|
Hypotrichosis Spanish Type
|
Hypotrichosis, Type 2
|
|
Hypotrichosis Simplex Of Scalp
|
|
|
| Familial Woolly Hair Syndrome |
|
Wooly Hair
|
Familial Wooly Hair Syndrome
|
|
Hereditary Woolly Hair Syndrome
|
Hereditary Wooly Hair Syndrome
|
|
Woolly Hair
|
Syndrome With Woolly Hair
|
|
Wooly Hair Syndrome
|
|
|
| Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive |
|
Hypohidrotic Ectodermal Dysplasia
|
Hed
|
|
Anhidrotic Ectodermal Dysplasia
|
Ectodermal Dysplasia, Hypohidrotic
|
|
Eda
|
Christ-Siemens-Touraine Syndrome
|
|
ECTD10B
|
Ectodermal Dysplasia Anhidrotic
|
|
Ectodermal Dysplasia, Anhidrotic
|
Cst Syndrome
|
|
Ectodermal Dysplasia Hypohidrotic Autosomal Recessive
|
Dysplasia, Ectodermal, Type 10b, Hypohidrotic/Hair/Tooth, Autosomal Recessive
|
|
Dysplasia, Ectodermal, Hypohidrotic
|
Ectodermal Dysplasia 11b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive
|
|
Ectodermal Dysplasia 3, Anhidrotic
|
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
|
|
|
