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Items: 8

1.

Emery-Dreifuss muscular dystrophy 1, X-linked

Emery-Dreifuss muscular dystrophy inherited in an X-linked recessive pattern and caused by mutations in the EMD gene, encoding emerin. [from NCI]

MedGen UID:
1720295
Concept ID:
C5243475
Disease or Syndrome
2.

Mandibuloacral dysplasia with type B lipodystrophy

Mandibuloacral dysplasia with type B lipodystrophy (MADB) is a rare autosomal recessive disorder characterized by postnatal growth retardation, craniofacial anomalies such as mandibular hypoplasia, skeletal anomalies such as progressive osteolysis of the terminal phalanges and clavicles, and skin changes such as mottled hyperpigmentation and atrophy. The lipodystrophy is characterized by generalized loss of subcutaneous fat involving the face, trunk, and extremities. Some patients have a progeroid appearance. Metabolic complications associated with insulin resistance have been reported (Schrander-Stumpel et al., 1992; summary by Simha et al., 2003). For a general phenotypic description of lipodystrophy associated with mandibuloacral dysplasia, see MADA (248370). [from OMIM]

MedGen UID:
332940
Concept ID:
C1837756
Disease or Syndrome
3.

Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2

Cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome (CAMRQ) is a genetically heterogeneous disorder characterized by congenital cerebellar ataxia and intellectual disability (summary by Gulsuner et al., 2011). For a discussion of genetic heterogeneity of CAMRQ, see CAMRQ1 (224050). [from OMIM]

MedGen UID:
412914
Concept ID:
C2750234
Disease or Syndrome
4.

Hypoparathyroidism - X-linked

A rare genetic hypoparathyroidism characterized by severe hypocalcemia, seizures, hyperphosphatemia, and undetectable parathyroid hormone levels, in the absence of parathyroid tissue. Complications include psychomotor and growth delay, delayed dentition, and cataracts. [from ORDO]

MedGen UID:
87437
Concept ID:
C0342344
Disease or Syndrome
5.

Odontotrichomelic syndrome

A rare genetic disease characterized by intellectual disability, growth delay, absence deformities of upper and lower limbs, hypotrichosis, hypoplastic nails, abnormal dentition, abnormal auricles, hypoplastic nipples, thyroid enlargement, and abnormalities of tyrosine and/or tryptophane metabolism. Hypogonadism and cleft lip have also been reported. No new cases have been confirmed since 1970. [from ORDO]

MedGen UID:
443944
Concept ID:
C2930960
Disease or Syndrome
6.

Congenital absence of cervical vertebra

Agenesis of one or more vertebrae of the cervical vertebral column. [from HPO]

MedGen UID:
140922
Concept ID:
C0432160
Congenital Abnormality
7.

Parotidomegaly, hereditary bilateral

MedGen UID:
401477
Concept ID:
C1868590
Disease or Syndrome
8.

Abnormality of the neck

An abnormality of the neck. [from HPO]

MedGen UID:
540042
Concept ID:
C0266623
Congenital Abnormality
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