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Term:
Parent Terms Term With Siblings Child Terms
absence of fingerprints-congenital milia syndrome 
acne +   
acrogeria 
A congenital skin condition characterized by premature aging, more especially in the form of unusually fragile, thin skin on the hands and feet. Its onset is in early childhood; it progresses over the next few years and then remains stable. A bruising tendency has been observed.
acrokeratosis verruciformis 
acroosteolysis-keloid-like lesions-premature aging syndrome 
albinism-hearing loss syndrome 
alopecia, isolated +  
aplasia cutis congenita +  
autosomal dominant vibratory urticaria 
autosomal recessive cutis laxa type 2A +  
Becker nevus syndrome +  
blue rubber bleb nevus 
body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency 
CHILD syndrome 
chorea-acanthocytosis 
chronic mucocutaneous candidiasis +  
CLOVES syndrome 
combined immunodeficiency with skin granulomas 
Cowden disease +  
cutaneous mastocytosis +   
Darier disease 
de Barsy syndrome +  
dermatitis herpetiformis, familial 
dermatosis papulosa nigra 
DK1-congenital disorder of glycosylation 
dyschromatosis universalis hereditaria +  
ectodermal dysplasia syndrome +   
encephalocraniocutaneous lipomatosis 
epidermodysplasia verruciformis +  
familial acanthosis nigricans 
familial acne inversa +  
familial chilblain lupus +  
familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome 
familial keratoacanthoma 
familial multiple fibrofolliculoma 
familial multiple nevi flammei 
familial pityriasis rubra pilaris 
familial primary localized cutaneous amyloidosis +  
Flynn-Aird syndrome 
generalized basaloid follicular hamartoma syndrome 
H syndrome 
Hailey-Hailey disease 
Hallermann-Streiff syndrome 
hereditary angioedema +  
hereditary lipodystrophy +  
hereditary mucoepithelial dysplasia 
hereditary mucosal leukokeratosis +  
hereditary palmoplantar keratoderma +  
hereditary papulotranslucent acrokeratoderma 
hereditary photodermatosis +  
hereditary sclerosing poikiloderma with tendon and pulmonary involvement 
hyperkeratosis-hyperpigmentation syndrome 
hyperpigmentation with or without hypopigmentation, familial progressive +  
inflammatory poikiloderma with hair abnormalities and acral keratoses 
inherited epidermolysis bullosa +  
inherited ichthyosis +  
isolated anhidrosis with normal sweat glands 
isolated congenital adermatoglyphia 
isolated hyperchlorhidrosis 
juvenile hyaline fibromatosis 
keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome 
keratosis pilaris atrophicans +  
lamellar ichthyosis +  
large congenital melanocytic nevus 
Legius syndrome 
lichen planus, familial 
lichen sclerosus et atrophicus +  
linear nevus sebaceous syndrome 
linear skin defects with multiple congenital anomalies 
lipoid proteinosis 
LMNA-related cardiocutaneous progeria syndrome 
Maffucci syndrome 
mandibular hypoplasia-deafness-progeroid syndrome 
MEDNIK syndrome 
monilethrix 
multiple benign circumferential skin creases on limbs 1 
neonatal inflammatory skin and bowel disease +  
neurocutaneous melanocytosis 
nevus comedonicus syndrome 
nevus, epidermal +  
oculocutaneous albinism +  
osteopathia striata-pigmentary dermopathy-white forelock syndrome 
PENS syndrome 
phakomatosis pigmentokeratotica 
piebaldism 
Pilomatrixoma 
poikiloderma with neutropenia 
porokeratosis +  
progeroid syndrome +  
Progeroid syndrome, Petty type 
progressive osseous heteroplasia 
psoriasis +   
reticulate pigment disorder +  
scalp defects-postaxial polydactyly syndrome 
schwannomatosis 
sebocystomatosis 
seborrhea-like dermatitis with psoriasiform elements 
seborrheic keratosis +   
segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome 
severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome 
Sneddon syndrome 
spinocerebellar ataxia type 34 
stiff skin syndrome 
Subcutaneous Panniculitis-Like T-Cell Lymphoma 
sweet syndrome 
syndromic oculocutaneous albinism +  
telomere syndrome +   
Tietz syndrome 
vasculitis, lymphocytic, nodular 
X-linked chondrodysplasia punctata 2 
X-linked reticulate pigmentary disorder 

Synonyms
Exact Synonyms: Gottron syndrome ;   Orphanet:2500 ;   acrogeria, Gottron type ;   acrometageria ;   http://identifiers.org/medgen/96063 ;   http://identifiers.org/mesh/C538187 ;   http://identifiers.org/snomedct/238872007 ;   http://linkedlifedata.com/resource/umls/id/C0406584 ;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1607996977 ;   https://omim.org/entry/201200
Related Synonyms: Metageria ;   familial acrogeria
Alternate IDs: MONDO:0008716
Xrefs: GARD:6543 ;   ICD9:259.8 ;   MEDGEN:96063 ;   MESH:C538187 ;   MIM:201200 ;   NORD:1202 ;   ORDO:2500 ;   SCTID:238872007 ;   UMLS:C0406584 ;   icd11.foundation:1607996977
Definition Sources: Wikipedia:Acrogeria

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