| Diseases |
Alias |
|
| Erythrokeratodermia Variabilis Et Progressiva 2 |
|
|
| Erythrokeratodermia Variabilis Et Progressiva 1 |
|
Erythrokeratodermia Variabilis
|
Erythrokeratodermia Variabilis Et Progressiva
|
|
Greither Disease
|
Ekv
|
|
Ekvp
|
PSEK
|
|
Erythrokeratodermia Variabilis With Erythema Gyratum Repens
|
Keratosis Palmoplantaris Transgrediens Et Progrediens
|
|
Transgrediens Et Progrediens Palmoplantar Keratoderma
|
EKVP1
|
|
Erythrokeratodermia, Progressive Symmetric
|
Erythrokeratodermia Figurata, Congenital Familial, In Plaques
|
|
Keratoderma Palmoplantaris Transgrediens
|
Keratosis Extremitatum Hereditaria Progrediens
|
|
Erythrokeratodermia Variabilis, Mendes Da Costa Type
|
Progressive Symmetric Erythrokeratodermia
|
|
Erythrokeratodermia Figurata Variabilis
|
Greither'S Disease
|
|
Ekv-P
|
Erythrokeratodermia Variabilis Of Mendes Da Costa
|
|
Progressive Symmetrical Erythrokeratoderma Of Gottron
|
Progressive Diffuse Ppk
|
|
Progressive Diffuse Palmoplantar Keratoderma
|
Transgrediens Et Progrediens Ppk
|
|
Darier-Gottron Disease
|
Erythrokeratodermia Progressiva Symmetrica
|
|
Progressive Symmetric Erythrokeratodermia, Gottron Type
|
Congenital Familial Erythrokeratodermia Figurata In Plaques
|
|
Erythrokeratodermia Progressive Symmetric
|
Erythrokeratodermia Variabilis Mendes Da Costa Type
|
|
|
| Erythrokeratoderma |
|
|
| Bart-Pumphrey Syndrome |
|
Knuckle Pads, Leukonychia, And Sensorineural Deafness
|
BAPS
|
|
Knuckle Pads, Leuconychia And Sensorineural Deafness
|
Knuckle Pads-Leukonychia-Sensorineural Deafness-Palmoplantar Hyperkeratosis Syndrome
|
|
Knuckle Pads-Leukonychia-Sensorineural Deafness-Palmoplantar Keratoderma Syndrome
|
Knuckle Pads, Deafness And Leukonychia Syndrome
|
|
Knuckle Pads, Deafness, And Leukonychia Syndrome
|
Knuckle Pads-Leukonychia-Sensorineural Hearing Loss-Palmoplantar Hyperkeratosis Syndrome
|
|
Knuckle Pads-Leukonychia-Sensorineural Hearing Loss-Palmoplantar Keratoderma Syndrome
|
|
|
| Palmoplantar Keratoderma And Congenital Alopecia 1 |
|
Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia
|
PPKCA1
|
|
Keratoderma-Hypotrichosis-Leukonychia Totalis Syndrome
|
Autosomal Dominant Palmoplantar Hyperkeratosis And Congenital Alopecia
|
|
Palmoplantar Keratoderma And Congenital Alopecia, Stevanovic Type
|
Ppk-Ca, Stevanovic Type
|
|
Ppkca, Stevanovic Type
|
Palmoplantar Keratoderma With Congenital Alopecia
|
|
Ppkca Stevanovic Type
|
Alopecia Congenita With Hyperkeratosis Of The Palms And Soles
|
|
Alopecia Congenita Keratosis Palmoplantaris
|
Keratoderma, Palmoplantar, With Congenital Alopecia, Type 1
|
|
|
| Hereditary Lymphedema Ic |
|
Lymphedema, Hereditary, Ic
|
Lmph1c
|
|
|
| Craniometaphyseal Dysplasia, Autosomal Recessive |
|
CMDR
|
Autosomal Recessive Craniometaphyseal Dysplasia
|
|
Craniometaphyseal Dysplasia, Autosomal Recessive Type
|
Dysplasia, Craniometaphyseal, Autosomal Recessive
|
|
|
| Keratoderma, Palmoplantar, With Deafness |
|
Palmoplantar Keratoderma-Deafness Syndrome
|
Palmoplantar Keratoderma With Deafness
|
|
Palmoplantar Hyperkeratosis-Deafness Syndrome
|
Palmoplantar Hyperkeratosis-Hearing Loss Syndrome
|
|
Palmoplantar Keratoderma-Hearing Loss Syndrome
|
Ppk-Deafness Syndrome
|
|
Keratoderma Palmoplantar Deafness
|
Diffuse Palmoplantar Keratoderma With Deafness
|
|
Focal Palmoplantar Keratoderma With Sensorineural Deafness
|
Hereditary Palmoplantar Keratoderma With Deafness
|
|
Keratoderma Palmoplantar, With Deafness
|
Palmoplantar Keratoderma And Sensorineural Deafness
|
|
Ppk With Deafness
|
PPKDFN
|
|
Keratoderma Palmoplantar, Deafness
|
|
|
| Skin Disease |
|
Skin Diseases
|
Genodermatosis
|
|
Abnormality Of The Skin
|
Skin Diseases, Genetic
|
|
Skin And Subcutaneous Tissue Disease
|
Dermatologic Disorders
|
|
|
| Clouston Syndrome |
|
Ectodermal Dysplasia 2, Clouston Type
|
Hidrotic Ectodermal Dysplasia
|
|
ECTD2
|
Clouston'S Hidrotic Ectodermal Dysplasia
|
|
Hidrotic Ectodermal Dysplasia Syndrome
|
Clouston Hidrotic Ectodermal Dysplasia
|
|
Clouston'S Syndrome
|
Ed2
|
|
Ectodermal Dysplasia, Hidrotic
|
Hed2
|
|
Ectodermal Dysplasia
|
Ectodermal Dysplasia, Hidrotic, Autosomal Dominant
|
|
Ectodermal Dysplasia, Hidrotic, 2, Formerly
|
Hed2, Formerly
|
|
Autosomal Dominant Hidrotic Ectodermal Dysplasia
|
Hed
|
|
Hidrotic Ectodermal Dysplasia, Autosomal Dominant
|
Hidrotic Ectodermal Dysplasia 2
|
|
Ectodermal Dysplasia 2 Hidrotic
|
Ectodermal Dysplasia Hidrotic Autosomal Dominant
|
|
Dysplasia, Ectodermal, Hidrotic
|
|
|
| Vohwinkel Syndrome |
|
Mutilating Keratoderma
|
Keratoderma Hereditarium Mutilans
|
|
Khm
|
VOWNKL
|
|
Deafness, Congenital, With Keratopachydermia And Constrictions Of Fingers And Toes
|
Mutilating Keratoderma Of Vohwinkel
|
|
Mutilating Keratoderma Plus Deafness
|
Ppk Mutilans And Deafness
|
|
Congenital Deafness With Keratopachydermia And Constrictions Of Fingers And Toes
|
Congenital Deafness With Keratopachydermia And Constrictions Fo Fingers And Toes
|
|
Palmoplantar Keratoderma Mutilans
|
Palmoplantar Keratoderma Mutilans Vohwinkel
|
|
Ppk Mutilans Vohwinkel
|
Mutilating Keratoderma Plus Hearing Loss
|
|
Ppk Mutilans And Hearing Loss
|
|
|
| Erythrasma |
|
Infection Due To Corynebacterium Minutissimum
|
|
|
| Oculodentodigital Dysplasia |
|
Odd Syndrome
|
ODDD
|
|
Oculodentoosseous Dysplasia
|
Oculodentodigital Syndrome
|
|
Odod
|
Oculo-Dento-Digital Dysplasia
|
|
Oculo-Dento-Digital Syndrome
|
Oculo-Dento-Osseous Dysplasia
|
|
Osseous-Oculo-Dental Dysplasia
|
Meyer-Schwickerath Syndrome
|
|
Oddd Syndrome
|
Oculo Dento Digital Dysplasia
|
|
Odds
|
Oculodentodigital Dysplasia Syndrome
|
|
|
| Ainhum |
|
Dactylolysis Spontanea
|
Spontaneous Dactylolysis
|
|
|
| Ectodermal Dysplasia |
|
Congenital Ectodermal Defect
|
Congenital Ectodermal Dysplasia
|
|
Ectodermal Dysplasia Syndrome
|
Dysplasia, Ectodermal
|
|
|
| Linear Skin Defects With Multiple Congenital Anomalies 1 |
|
Midas Syndrome
|
Mcops7
|
|
Mls Syndrome
|
Microphthalmia, Syndromic 7
|
|
Microphthalmia With Linear Skin Defects Syndrome
|
Microphthalmia With Linear Skin Defects
|
|
Microphthalmia-Dermal Aplasia-Sclerocornea Syndrome
|
Syndromic Microphthalmia Type 7
|
|
LSDMCA1
|
Mls
|
|
Microphthalmia, Dermal Aplasia, And Sclerocornea
|
Microphthalmia With Linear Skin Defect Syndrome
|
|
Syndromic Microphthalmia 7
|
Linear Skin Defects With Multiple Congenital Anomalies
|
|
Microphthalmia, Dermal Aplasia, Sclerocornea Syndrome
|
Microphthalmia Dermal Aplasia And Sclerocornea Syndrome
|
|
Micropthalmia Syndromic 7
|
Microphthalmia Syndromic 7
|
|
Microphthalmia With Linear Skin Lesions Syndrome
|
Syndromic Microphthalmia-7
|
|
Microphthalmia, Dermal Aplasia And Sclerocornea
|
Microphthalmia, Syndromic, 7
|
|
Midas
|
|
|
| Cataract 1, Multiple Types |
|
Cataract 1 Multiple Types
|
CTRCT1
|
|
Cataract 1, Multiple Types, With Or Without Microcornea
|
Czp1
|
|
Cae1
|
Pulverulent Zonular Cataract
|
|
Cataract, Duffy-Linked
|
Cataract, Zonular Pulverulent, 1
|
|
Duffy Linked Cataract
|
Zonular Pulverulent Cataract 1
|
|
Cataract Duffy-Linked
|
Cataract-Microcornea Syndrome
|
|
Cataract Zonular Pulverulent 1
|
Ccmc
|
|
Cznp
|
Czp
|
|
Zonular Nuclear Pulverulent Cataract
|
Cataract, Zonular Pulverulent-1
|
|
Zonular Pulverulent Cataract
|
Cataract, Zonular Pulverulent 1
|
|
Cataract Microcornea Syndrome
|
|
|
| Albinism, Ocular, With Late-Onset Sensorineural Deafness |
|
Ocular Albinism With Sensorineural Deafness
|
OASD
|
|
Deafness And Ocular Albinism
|
Ocular Albinism With Late-Onset Sensorineural Deafness
|
|
Albinism, Ocular, With Sensorineural Deafness
|
Autosomal Recessive Waardenburg Syndrome Type 2 With Ocular Albinism
|
|
Digenic Waardenburg Syndrome/Albinism
|
Digenic Waardenburg Syndrome/Ocular Albinism
|
|
Ws2-Oa
|
Albinism Ocular Late Onset Sensorineural Deafness
|
|
Ocular Albinism With Late-Onset Sensorineural Hearing Loss
|
Waardenburg Syndrome/Ocular Albinism, Digenic
|
|
Waardenburg Syndrome/Albinism, Digenic
|
Ocular Albinism And Sensorineural Deafness
|
|
|
| Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, And Keratoderma |
|
Mednik Syndrome
|
Erythrokeratodermia Variabilis 3
|
|
MEDNIK
|
Ekv3
|
|
Erythrokeratodermia Variabilis, Kamouraska Type
|
Mental Retardation, Enteropathy, Deafness, Neuropathy, Ichthyosis, Keratodermia
|
|
Intellectual Disability-Enteropathy-Deafness-Peripheral Neuropathy-Ichthyosis-Keratodermia Syndrome
|
Intellectual Disability-Enteropathy-Hearing Loss-Peripheral Neuropathy-Ichthyosis-Keratodermia Syndrome
|
|
Intellectual Disability, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, And Keratoderma
|
Erythrokeratodermia Variabilis Kamouraska Type
|
|
Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, Keratoderma
|
|
|
| Palmoplantar Keratosis |
|
Palmoplantar Keratoderma
|
Keratosis Palmaris Et Plantaris
|
|
Palmo-Plantar Keratodermas
|
Keratoderma, Palmoplantar
|
|
Keratoderma Palmoplantar
|
Keratoderma, Palmoplantar, Diffuse
|
|
Hyperkeratosis Of Palms And Soles
|
Palmoplantar Hyperkeratosis
|
|
|
| Leukodystrophy, Hypomyelinating, 2 |
|
Pmld1
|
Hypomyelinating Leukodystrophy 2
|
|
HLD2
|
Pelizaeus-Merzbacher-Like Disease 1
|
|
Pelizaeus-Merzbacher-Like Disease Due To Gjc2 Mutation
|
Pelizaeus-Merzbacher-Like Disease Type 1
|
|
Pelizaeus-Merzbacher-Like Disease, 1
|
Pelizaeus Merzbacher Like Disease
|
|
Pelizaeus-Merzbacher-Like Disease
|
Pmld - Pelizaeus Merzbacher Like Disease
|
|
Pelizaeus-Merzbacher-Like Disease Autosomal Recessive Type 1
|
Pmldar1
|
|
Leukodystrophy, Hypomyelinating, Type 2
|
|
|
| Exposure Keratitis |
|
Exposure Keratoconjunctivitis
|
Lagophthalmic Keratitis
|
|
|
| Nevus, Epidermal |
|
Epidermal Nevus
|
Woolly Hair Nevus
|
|
Epidermal Naevus
|
Epidermal Nevus Syndrome
|
|
Nevus, Keratinocytic, Nonepidermolytic
|
Epidermal Nevus, Somatic
|
|
Nevus, Epidermal, Somatic
|
Nevus Sebaceous Or Woolly Hair Nevus, Somatic
|
|
Nonepidermolytic Keratinocytic Nevus
|
Epidermal Hamartoma Syndrome
|
|
Wooly Hair Nevus
|
Keratinocytic Non-Epidermolytic Nevus
|
|
KNEN
|
Pigmented Moles
|
|
Organoid Nevus Phakomatosis
|
Nevus Sebaceous
|
|
Melanocytic Nevus
|
Melanocytic Nevus Of Skin
|
|
|
| Cornelia De Lange Syndrome 1 |
|
De Lange Syndrome
|
CDLS1
|
|
Cdl
|
Cdls
|
|
Typus Degenerativus Amstelodamensis
|
Brachmann-De Lange Syndrome
|
|
Bdls
|
Amstelodamensis Typus Degenerativus
|
|
Cornelia De Lange Syndrome, Type 1
|
|
|
| Autosomal Recessive Congenital Ichthyosis |
|
Lamellar Ichthyosis
|
Congenital Ichthyosiform Erythroderma
|
|
Li
|
Congenital Nonbullous Ichthyosiform Erythroderma
|
|
Arci
|
Congenital Lamellar Ichthyosis
|
|
Nonbullous Congenital Ichthyosiform Erythroderma
|
Cie
|
|
Congenital Non-Bullous Ichthyosiform Erythroderma
|
Erythrodermic Ichthyosis
|
|
Nbcie
|
Ncie
|
|
Non-Bullous Congenital Ichthyosiform Erythroderma
|
Collodion Baby
|
|
Ichthyosis, Lamellar
|
Non Bullous Congenital Ichthyosiform Erythroderma
|
|
Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form
|
Ichthyosiform Erythroderma, Congenital, Nonbullous, 1
|
|
Collodion Baby Syndrome
|
Ichthyoses, Lamellar
|
|
Nbie
|
Nonbullous Ichthyosiform Erythroderma
|
|
Classic Lamellar Ichthyosis
|
Ichthyosiform Erythroderma Nonbullous Congenital
|
|
Ichthyosiform Erythroderma Congenital
|
Ichthyosis, Congenital, Autosomal Recessive
|
|
Ichthyosiform Erythroderma, Congenital
|
Collodion Fetus
|
|
Non-Bullous Ichthyosiform Erythroderma
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
