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Focal Dermal Hypoplasia
Focal dermal hypoplasia
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Genodermatoses
(157)
Aplasia cutis congenita
Bloom syndrome
CHILD syndrome
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Dermatopathia pigmentosa reticularis
Epidermolysis bullosa dystrophica
Epidermolysis bullosa simplex
Epidermolytic hyperkeratosis
Familial cutaneous papillomatosis
Harlequin type ichthyosis
Hay-Wells syndrome
Hypohidrotic ectodermal dysplasia
Ichthyosis lamellaris
Incontinentia pigmenti
Kindler syndrome
Lelis syndrome
Meleda Disease
Naegeli syndrome
Netherton syndrome
X-linked ichthyosis
Zunich Kaye syndrome
18q deletion syndrome
Acrocephal- osyndactylia
Acrodermatitis enteropathica
Acrokeratosis verruciformis
Adams–Oliver syndrome
Adducted thumbs syndrome
Albright's hereditary osteodystrophy
Apert syndrome
Arrhythmogenic right ventricular dysplasia
Ataxia telangiectasia
Atrichia with papular lesions
Atrophodermia vermiculata
Autoimmune polyendocr- inopathy–candidiasis–ectodermal dystrophy syndrome
BIDS syndrome
Bart syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
Conradi–Hünermann syndrome
Costello syndrome
Cronkhite-Canada syndrome
Crouzon syndrome
Cutis verticis gyrata
Darier's disease
Disseminated superficial actinic porokeratosis
Disseminated superficial porokeratosis
Dominant dystrophic epidermolysis bullosa
Dyschromatosis universalis hereditaria
Dyskeratosis congenita
Ectodermal dysplasia
Ectodermal dysplasia with corkscrew hairs
Ectrodacty- ly-ectodermal dysplasia-cleft syndrome
Epidermolysis bullosa
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Erythrokeratodermia variabilis
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Follicular atrophoderma
Franceschetti–Klein syndrome
Freeman-Sheldon syndrome
Generalized atrophic benign epidermolysis bullosa
Generalized epidermolysis bullosa simplex
Generalized trichoepithelioma
Hailey-Hailey disease
Hallermann-Streiff syndrome
Hereditary sclerosing poikiloderma
IBIDS syndrome
IFAP syndrome
Ichthyosis
Ichthyosis bullosa of Siemens
Ichthyosis hystrix
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
IgA pemphigus
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
Keratosis follicularis spinulosa decalvans
Keratosis pilaris
Keratosis pilaris atrophicans faciei
Klinefelter's syndrome
Klippel–Feil syndrome
LEOPARD syndrome
Lentiginosis
Lenz–Majewski syndrome
Linear Darier disease
Linear and whorled nevoid hypermelanosis
Linear porokeratosis
Localized epidermolysis bullosa simplex
Mandibuloacral dysplasia
Marinesco–Sjögren syndrome
McCusick syndrome
Mitis junctional epidermolysis bullosa
Multiple sulfatase deficiency
Neurofibromatosis
Neurofibromatosis type 3
Neurofibromatosis type 4
Neurofibromatosis type I
Neutral lipid storage disease
Noonan syndrome
Odonto–T- richo–Ungual–Digital–Palmar syndrome
PIBI(D)S syndrome
POEMS syndrome
Pachydermo- periostosis
Pachyonychia congenita
Pachyonychia congenita type I
Pachyonychia congenita type II
Papillon–Lefèvre syndrome
Peeling skin syndrome
Pfeiffer syndrome
Pityriasis rotunda
Plaque-type porokeratosis
Polyostotic fibrous dysplasia
Popliteal pterygium syndrome
Porokeratosis
Porokeratosis palmaris et plantaris disseminata
Progeria
Progressive symmetric erythrokeratodermia
Proteus syndrome
Punctate porokeratosis
Rapp–Hodgkin syndrome
Recessive dystrophic epidermolysis bullosa
Refsum's disease
Relapsing linear acantholytic dermatosis
Restrictive dermopathy
Rhizomelic chondrodysplasia punctata
Rombo syndrome
Rothmund–Thomson syndrome
Scleroatrophic syndrome of Huriez
Sjögren–Larsson syndrome
Tooth and nail syndrome
Transient bullous dermolysis of the newborn
Treacher Collins syndrome
Tricho–r- hino–phalangeal syndrome
Tuberous sclerosis
Turner syndrome
Ulerythema
Ulnar–mammary syndrome
Von Hippel – Lindau disease
Watson syndrome
Werner syndrome
Westerhof syndrome
Wilson–Turner syndrome
Wolf–Hirschhorn syndrome
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Xeroderma pigmentosum
Zimmermann–Laband syndrome
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Diseases and disorders
(46)
Syndromes
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
MASA syndrome
MASA syndrome
Goltz-Gorlin syndrome
X-linked sideroblastic anemia
Lipid storage disorder
Becker's muscular dystrophy
Pyruvate dehydrogenase deficiency
Hypoplasia
Alport syndrome
X-linked hypophosphatemia
X-linked lymphoproliferative disease
Barth syndrome
Androgen insensitivity syndrome
Adenosine deaminase deficiency
Haemophilia
Cutis laxa
22q11.2 deletion syndrome
Hematologic disease
Fibromatosis
Microphthalmia
Acanthosis nigricans
Agenesis of the corpus callosum
Wiskott-aldrich syndrome
Diaphragmatic hernia
Fabry disease
Skin cancer
Mental retardation
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Dermatopathia pigmentosa reticularis
Epidermolysis bullosa dystrophica
Naegeli syndrome
Hay-Wells syndrome
X-linked ichthyosis
Bloom syndrome
Harlequin type ichthyosis
Hypohidrotic ectodermal dysplasia
Incontinentia pigmenti
Aplasia cutis congenita
Epidermolysis bullosa simplex
Netherton syndrome
CHILD syndrome
more...
Syndromes
(12)
McLeod syndrome
Fg syndrome
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Zunich Kaye syndrome
Naegeli syndrome
Hay-Wells syndrome
Alport syndrome
Bloom syndrome
Androgen insensitivity syndrome
Netherton syndrome
22q11.2 deletion syndrome
more...
Autosomal recessive disorders
(14)
Finnish heritage disease
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
Zunich Kaye syndrome
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Kindler syndrome
Lipid storage disorder
Bloom syndrome
Harlequin type ichthyosis
Netherton syndrome
Adenosine deaminase deficiency
more...
Abnormalities of dermal fibrous and elastic tissue
Acrodermatitis Chronica Atrophicans
Gerodermia osteodysplastica
Cutis laxa
Genetics
X linked
X-linked recessive
Mutations
Mosaicism
Genetic disorders
(35)
Aicardi syndrome
Adrenoleuk- odystrophy
X-linked dominant
Lelis syndrome
Familial cutaneous papillomatosis
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
Zunich Kaye syndrome
Ichthyosis lamellaris
MASA syndrome
Goltz-Gorlin syndrome
Congenital ichthyosiform erythroderma
X-linked sideroblastic anemia
Dermatopathia pigmentosa reticularis
Kindler syndrome
Lipid storage disorder
Finnish heritage disease
Becker's muscular dystrophy
Simpson-Go- labi-Behmel syndrome
Pyruvate dehydrogenase deficiency
McLeod syndrome
Hay-Wells syndrome
Alport syndrome
Bloom syndrome
Fg syndrome
Barth syndrome
Androgen insensitivity syndrome
Netherton syndrome
Adenosine deaminase deficiency
Haemophilia
22q11.2 deletion syndrome
Microphthalmia
Wiskott-aldrich syndrome
Fabry disease
more...
See also
(20)
Nevus flammeus nuchae
Papulosquamous hyperkeratotic skin diseases
Hyper IgM Syndrome Type 1
Congenital malformations
PORCN
PORCN
Autosomal dominant
Autosomal recessive
Simpson-Go- labi-Behmel syndrome
Integument
Subcutaneous tissue
Cadherin
Autosomal
Birthmarks
Immune disorders
Skin lesion
KAL1
Atrophic
Acral Acanthotic Anomaly
Blaschko
J. Am. Acad. Dermatol.
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