Erythrokeratodermia

Erythrokeratodermia is a group of keratinization disorders.[1]

Types include:

References

"Erythrokeratoderma - DermNet New Zealand". www.dermnet.org.nz.

Congenital malformations and deformations of integument / skin disease

Congenital ichthyosis/
erythrokeratodermia

AD	Ichthyosis vulgaris
AR	Congenital ichthyosiform erythroderma: Epidermolytic hyperkeratosis Lamellar ichthyosis Harlequin-type ichthyosis Netherton syndrome Zunich–Kaye syndrome Sjögren–Larsson syndrome
XR	X-linked ichthyosis
Ungrouped	Ichthyosis bullosa of Siemens Ichthyosis follicularis Ichthyosis prematurity syndrome Ichthyosis–sclerosing cholangitis syndrome Nonbullous congenital ichthyosiform erythroderma Ichthyosis linearis circumflexa Ichthyosis hystrix

EB
and related

EBS
- EBS-K
- EBS-WC
- EBS-DM
- EBS-OG
- EBS-MD
- EBS-MP

JEB
- JEB-H
- Mitis
- Generalized atrophic
- JEB-PA

DEB
- DDEB
- RDEB

Ectodermal dysplasia

Elastic/Connective

Hyperkeratosis/
keratinopathy

diffuse: Diffuse epidermolytic palmoplantar keratoderma
Diffuse nonepidermolytic palmoplantar keratoderma
Palmoplantar keratoderma of Sybert
Meleda disease

syndromic
- connexin
  - Bart–Pumphrey syndrome
  - Clouston's hidrotic ectodermal dysplasia
  - Vohwinkel syndrome
- Corneodermatoosseous syndrome
- plakoglobin
  - Naxos syndrome
- Scleroatrophic syndrome of Huriez
- Olmsted syndrome
- Cathepsin C
  - Papillon–Lefèvre syndrome
  - Haim–Munk syndrome
- Camisa disease
- focal: Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
- Focal palmoplantar and gingival keratosis
- Howel–Evans syndrome
- Pachyonychia congenita
  - Pachyonychia congenita type I
  - Pachyonychia congenita type II
- Striate palmoplantar keratoderma
- Tyrosinemia type II

punctate: Acrokeratoelastoidosis of Costa
Focal acral hyperkeratosis
Keratosis punctata palmaris et plantaris
Keratosis punctata of the palmar creases
Schöpf–Schulz–Passarge syndrome
Porokeratosis plantaris discreta
Spiny keratoderma

ungrouped: Palmoplantar keratoderma and spastic paraplegia
desmoplakin
- Carvajal syndrome
connexin
- Erythrokeratodermia variabilis
- HID/KID

Other

Other

see also Template:Congenital malformations and deformations of skin appendages, Template:Phakomatoses, Template:Pigmentation disorders, Template:DNA replication and repair-deficiency disorder

Developmental
anomalies

Midline	Dermoid cyst Encephalocele Nasal glioma PHACE association Sinus pericranii
Nevus	Capillary hemangioma Port-wine stain Nevus flammeus nuchae
Other/ungrouped	Aplasia cutis congenita Amniotic band syndrome Branchial cyst Cavernous venous malformation Accessory nail of the fifth toe Bronchogenic cyst Congenital cartilaginous rest of the neck Congenital hypertrophy of the lateral fold of the hallux Congenital lip pit Congenital malformations of the dermatoglyphs Congenital preauricular fistula Congenital smooth muscle hamartoma Cystic lymphatic malformation Median raphe cyst Melanotic neuroectodermal tumor of infancy Mongolian spot Nasolacrimal duct cyst Omphalomesenteric duct cyst Poland anomaly Rapidly involuting congenital hemangioma Rosenthal–Kloepfer syndrome Skin dimple Superficial lymphatic malformation Thyroglossal duct cyst Verrucous vascular malformation Birthmark

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