Amniotic constriction ring

Symptom Information:

Symptom ID: HPO:0009775
Synonyms:
Amniotic bands [HPO:0009775]
Amniotic constriction band [HPO:0009775]
Pseudoainhum [HPO:0009775]
Constriction ring [Orphanet:18880]
Amniotic bands [OMIM:Amniotic bands]
Pseudoainhum [OMIM:Pseudoainhum]
Cutaneous/amniotic bands/webbing of joints [Orphanet:18880]
Joint web [Orphanet:18880]
Quality:
Cross references:
HPO:0010483 "Amniotic constriction rings of arms" [Orphanet:18880]
Orphanet:18880 "Cutaneous/amniotic bands/webbing of joints" [Orphanet:18880]
OMIM: "Amniotic bands" [OMIM:Amniotic bands]
OMIM: "Pseudoainhum" [OMIM:Pseudoainhum]
Is a (Direct Parents):
HPO         Abnormality of placental membranes
Orphanet Aplasia/hypoplasia of the extremities
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of prenatal development or birth(HPO:0001197)
          Abnormalities of placenta or umbilical cord(HPO:0001194)
             Abnormality of placental membranes(HPO:0011409)
                Amniotic constriction ring(HPO:0009775)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

AINHUM (OMIM:103400)
Absence of fingerprints - congenital milia (Orphanet:1658)
Amniotic bands (Orphanet:1034)
Ankyloblepharon filiforme adnatum - cleft palate (Orphanet:1072)
Antecubital pterygium syndrome (Orphanet:2987)
Arthrogryposis multiplex congenita (Orphanet:1037)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
Bowed tibiae - radial anomalies - osteopenia - fractures (Orphanet:3331)
CHILD syndrome (Orphanet:139)
Embryonary disorganization syndrome (Orphanet:1664)
Hereditary acrokeratotic poikiloderma of Kindler-Weary (Orphanet:306539)
Humerus trochlea aplasia (Orphanet:3383)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Keratoderma hereditarium mutilans (Orphanet:494)
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome (Orphanet:281201)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lethal multiple pterygium syndrome (Orphanet:33108)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
PHAVER syndrome (Orphanet:2876)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)