Milia

Symptom Information:

Symptom ID: HPO:0001056
Synonyms:
Milium [Orphanet:23300]
Closed comedone (disorder) [Orphanet:23300]
Milia (disorder) [Orphanet:23300]
Milial cyst (disorder) [Orphanet:23300]
Milium (morphologic abnormality) [Orphanet:23300]
Closed comedone [Orphanet:23300]
Milium Cyst [Orphanet:23300]
Milia [OMIM:Milia]
Follicular/erythematous/edematous papules/milium [Orphanet:23300]
Whiteheads [Orphanet:23300]
Milia [Orphanet:23300]
Milia [MedDRA:10027626]
Whiteheads [MedDRA:10027626]
Milia (less common) [OMIM:Milia (less common)]
Milia (rare) [OMIM:Milia (rare)]
Erythematous papules [Orphanet:23300]
Follicular papules [Orphanet:23300]
Follicular papule (morphologic abnormality) [Orphanet:23300]
Follicular papule [Orphanet:23300]
Follicular papules [OMIM:Follicular papules]
Edematous papules [Orphanet:23300]
Quality:
Cross references:
Orphanet:23300 "Follicular/erythematous/edematous papules/milium" [Orphanet:23300]
OMIM: "Milia" [OMIM:Milia]
OMIM: "Milia (less common)" [OMIM:Milia (less common)]
OMIM: "Milia (rare)" [OMIM:Milia (rare)]
OMIM: "Follicular papules" [OMIM:Follicular papules]
UMLS:C0345996 "Milia" [HPO:0001056]
UMLS:C0302302 "Closed comedone" [Orphanet:23300]
UMLS:C0345996 "Milium Cyst" [Orphanet:23300]
UMLS:C0332565 "Follicular papule" [Orphanet:23300]
Is a (Direct Parents):
MedDRA Apocrine and eccrine gland disorders
HPO         Localized skin lesion
Orphanet Abnormality of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Localized skin lesion(HPO:0011355)
                Milia(HPO:0001056)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Apocrine and eccrine gland disorders(MedDRA:10002982)
          Milia(HPO:0001056)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

Absence of fingerprints - congenital milia (Orphanet:1658)
Atrophoderma vermiculata (Orphanet:79100)
BROOKE-SPIEGLER SYNDROME (OMIM:605041)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Buschke-Ollendorff syndrome (Orphanet:1306)
Dystrophic epidermolysis bullosa pruriginosa (Orphanet:89843)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Generalized dominant dystrophic epidermolysis bullosa (Orphanet:231568)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Gorlin syndrome (Orphanet:377)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
Localized epidermolysis bullosa simplex (Orphanet:79400)
MILIA, MULTIPLE ERUPTIVE (OMIM:157400)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Orofaciodigital syndrome type 9 (Orphanet:141007)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Rosaï-Dorfman disease (Orphanet:158014)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Transient bullous dermolysis of the newborn (Orphanet:79411)
Tyrosinemia type 2 (Orphanet:28378)